BMJ 1998;316:1483-1487 ( 16 May )

Papers

Differences in late fetal death rates in association with determinants of small for gestational age fetuses: population based cohort study

Sven Cnattingius, associate professora Bengt Haglund, associate professorb Michael S Kramer, professorc

a Department of Medical Epidemiology, Karolinska Institute, S-171 77 Stockholm, Sweden, b Centre for Epidemiology, National Board of Health and Welfare, Stockholm, Sweden, c Department of Pediatrics, McGill University Faculty of Medicine, Montreal, Quebec, Canada

Correspondence to: Dr Cnattingius sven.cnattingius{at}epic.mep.ki.se

    Abstract
Top
Abstract
Introduction
Subjects and methods
Results
Discussion
References

Objective: To examine differences in late fetal death rates in association with determinants of small for gestational age fetuses.
Design: Population based cohort study.
Subjects: 1 026 249 pregnancies without congenital malformations.
Setting: Sweden 1983-92. 
Main outcome measure: Late fetal death rate.
Results: Depending on underlying determinants late fetal death rates were greatly increased in extremely small for gestational age fetuses (range 16 to 45 per 1000) compared with non-small for gestational age fetuses (1.4 to 4.6). In extremely small for gestational age fetuses late fetal death rates were increased from 31 per 1000 in mothers aged less than 35 years to 45 per 1000 in older mothers, and from 22 per 1000 in women <155 cm in height to 33 per 1000 in women >= 175 cm tall. Late fetal death rates were also higher in extremely small for gestational age fetuses in singleton compared with twin pregnancies and in non-hypertensive pregnancies compared with pregnancies complicated by severe pre-eclampsia or other hypertensive disorders. Slightly higher late fetal death rates were observed in nulliparous compared with parous women and in non-smokers compared with smokers.
Conclusions: Although the risk of late fetal death is greatly increased in fetuses that are extremely small for gestational age the risk is strongly modified by underlying determinants---for example, there is a lower risk of late fetal death in a small for gestational age fetus if the mother is of short stature, has a twin pregnancy, or has hypertension.

Key messages

  • Small for gestational age fetuses are at increased risk of late fetal death regardless of the underlying determinants

  • The effect of birthweight ratio on risk of late fetal death is modified by underlying determinants, except maternal age

  • Regardless of birthweight ratio the rates of late fetal death are higher among women aged 35 years or older compared with younger women

  • In pregnancies of extremely small for gestational age fetuses lower rates of late fetal death are associated with a maternal age of less than 35 years, short maternal stature, multiple births, and hypertensive disorders

  • In pregnancies with non-malformed fetuses late fetal death rates are increased in smokers, in multiple births, and in women with severe pre-eclampsia.


    Introduction
Top
Abstract
Introduction
Subjects and methods
Results
Discussion
References

A wide range of risk factors are associated with fetuses being small for gestational age,1 and the prognosis for such fetuses varies according to the presence of chromosomal or other congenital malformations.2-4 In pregnancies of small for gestational age fetuses without congenital malformations it has been assumed that constitutionally small fetuses---for example, twins, or infants born to short mothers---are at lower risk of adverse outcomes than fetuses affected by other situations such as pre-eclampsia or cigarette consumption. 5 6 In fact, such an assumption underlies recent pleas for customised or individualised definitions of a fetus being small for gestational age. 7 8 Unfortunately, this assumption has rarely been critically tested. 9 10

In Sweden the population based birth register includes information on risk factors for fetuses being small for gestational age including maternal age, height, parity, smoking habits, blood pressure status, and type of pregnancy (single or multiple). We used this information to study the differences in late fetal death rates in association with fetal size and underlying determinants of a fetus being small for gestational age.

    Subjects and methods
Top
Abstract
Introduction
Subjects and methods
Results
Discussion
References

Swedish birth register
In Sweden data from all hospital births, including demographics, reproductive history, and complications during pregnancy and delivery, are collected prospectively and recorded in a birth register.11 From 1983 to 1992 1 083 367 births were recorded. Our study was restricted to singleton or twin pregnancies without congenital malformations, according to ICD-8 (international classification of diseases, 8th revision) and ICD-9 (9th revision) codes 740-759, in women aged 15 to 44 years (n=1 026 249).

Maternal height and smoking habits are recorded at the time of registration for antenatal care. Parity is defined as the number of previous births, including stillbirths. Maternal age is defined as completed years at delivery. Any maternal disorders are noted by an obstetrician at the time of the woman's discharge. Hypertension is defined as12: essential (ICD-8 code 401 and ICD-9 codes 642A-C); gestational (non-proteinuric) (ICD-8 code 637.01 and ICD-9 codes 640D and 642X); mild (proteinuric) pre-eclampsia (ICD-8 code 637.03 and ICD-9 code 642E); severe (proteinuric) pre-eclampsia (ICD-8 code 637.04 and ICD-9 code 642F); and eclampsia (ICD-8 code 637.1 and ICD-9 code 642G). The 250 women with eclampsia were grouped with 5145 women with severe pre-eclampsia.

Birthweight ratio was defined as the ratio of observed to expected birth weight on the basis of the fetuses' gestational age and sex. Explanatory variables were the fetuses' sex, a third degree polynomial of gestational age in days, and interaction between the fetuses' sex and gestational age. A normal birthweight ratio was defined as >= 0.90 and that of mildly and extremely small for gestational age fetuses as >0.75 but <0.90 or =<0.75 respectively. Late fetal death was defined as a stillbirth delivered at 28 completed weeks of gestation or later. When available, ultrasonography was used to estimate gestational age during the second trimester otherwise gestational age was estimated from the last menstrual period. At the start of the study 50% of the obstetric departments performed routine ultrasonography. From 1990 onwards all pregnant women in Sweden were offered ultrasonography before 18 weeks' gestation. 13 14

We used multiple logistic regression analyses to estimate the effect of independent variables on late fetal death.

    Results
Top
Abstract
Introduction
Subjects and methods
Results
Discussion
References

Risk factors
Late fetal death rates were increased in women who were 35 years or older, were nulliparous, smoked, or were <155 cm in height (table 1). Essential hypertension, severe pre-eclampsia, and twin pregnancies were associated with greatly increased late fetal death rates. In pregnancies of normal birthweight ratio the late fetal death rate was 2.1 per 1000 compared with 4.7 and 32.8 per 1000 in pregnancies of mildly and extremely small for gestational age fetuses respectively.

                              
View this table:
[in this window]
[in a new window]
 

Table 1 Number of births and late fetal deaths associated with maternal characteristics, type of birth, and birthweight ratio in Sweden from 1983 to1992

Table 1 shows the relation between maternal and fetal characteristics and birthweight ratio. Maternal smoking habits and height influenced the mean birthweight ratio in a dose dependent manner but the largest effects were observed in women with severe pre-eclampsia or twin pregnancies.

Late fetal death rates and mean birthweight ratios were similar for women aged 20-24, 25-29, and 30-34 years. Compared with severe pre-eclampsia other hypertensive disorders were either uncommon or had a comparatively small influence on late fetal death or birthweight ratio. In the logistic regression analyses maternal age was grouped as 15-19, 20-34, and 35-44 years, and hypertension as none, severe pre-eclampsia, and other hypertensive disorders. Multiple logistic regression analyses showed that there was an increased risk of late fetal death in women who were 35 years or older, were nulliparous, smoked, had twin pregnancies, or had severe pre-eclampsia (table 2).

                              
View this table:
[in this window]
[in a new window]
 

Table 2 Adjusted odds ratios (95% confidence intervals) of late fetal death compared with maternal characteristics of women recorded in the Swedish birth register from 1983 to 1992 

In a second logistic model we estimated the crude effect of being small for gestational age on the risk of late fetal death. Compared with fetuses of a normal birthweight ratio the risk was doubled in fetuses mildly small for gestational age (odds ratio 2.3, 95% confidence interval 2.1 to 2.5) and greatly increased in fetuses extremely small for gestational age (16.5, 15.2 to 17.9).

Risk factors and birthweight ratio
To determine whether the increased risk of late fetal death related to a fetus being small for gestational age was modified by underlying determinants, we introduced interaction terms in the logistic regression models. Important interaction terms were found between birthweight ratio and all determinants studied except maternal age, and predicted rates of late fetal death were calculated as a function of birthweight ratio and its determinants (table 3). In extremely small for gestational age fetuses late fetal death rates ranged from 16 to 45 per 1000, which varied according to underlying determinants. In mildly small for gestational age fetuses late fetal death rates ranged from 2.3 to 8.7 per 1000, and from 1.3 to 4.6 per 1000 in fetuses of a normal birthweight ratio.

                              
View this table:
[in this window]
[in a new window]
 

Table 3 Adjusted rates and 95% confidence intervals of late fetal death compared with characteristics of pregnancy and birthweight ratio based on multiple logistic regression. Model includes significant interactions between risk factors and birthweight ratio

In extremely small for gestational age fetuses the predicted late fetal death rate was 33.1 per 1000 in women aged less than 35 years v 44.9 per 1000 in older women. Late fetal death rates also increased with maternal height, and were higher in singletons compared with twins and in non-hypertensive pregnancies compared with pregnancies complicated by hypertensive disorders. Slightly higher late fetal death rates were also observed in nulliparous women and in non-smokers. In mildly small for gestational age fetuses late fetal death rates were increased in women who were 35 years or older, were >= 155 cm in height, had twin pregnancies, or had severe pre-eclampsia. In fetuses of a normal birthweight ratio late fetal death rates were increased among women who were 35 years or older, were <155 cm in height, were nulliparous, smoked, had twin pregnancies, or had severe pre-eclampsia. Of the late fetal deaths, 51% were in the preterm period and 49% were at or after term. When the analyses in table 3 were restricted to full term pregnancies late fetal death rates were reduced: 0.9 per 1000 in non-small for gestational age fetuses and 2.3 and 9.8 in mildly and extremely small for gestational age fetuses respectively. The comparative increase in late fetal death rates by risk factors and birthweight ratio, however, remained unchanged (data not shown).

The impact of maternal height on late fetal death rate is shown when using birthweight ratio as a continuous variable (figure). Late fetal death rates consistently increased with decreasing birthweight ratio regardless of maternal height, but the increase was most pronounced among women >= 175 cm in height.


View larger version (18K):
[in this window]
[in a new window]
 
Rates of late fetal death compared with maternal height and birthweight ratio

    Discussion
Top
Abstract
Introduction
Subjects and methods
Results
Discussion
References

This study shows that late fetal death rates associated with a fetus being extremely small for gestational age are low in women who are less than 35 years, =<155 cm in height, have twin pregnancies, or have severe pre-eclampsia or other hypertensive disorders. Hypertensive disorders are well documented determinants of a fetus being small for gestational age, and close antenatal supervision may contribute to the favourable prognosis in these pregnancies. The reduced risks associated with short stature and multiple births, however, support the assumption that a small for gestational age fetus may be the result of constitutional rather than pathological factors.5-8 Even in short mothers, however, late fetal death rates were more than 10-fold higher in extremely small for gestational age fetuses compared with fetuses of a normal birthweight ratio clearly indicating that even in short mothers the consequences of a fetus being small for gestational age may be serious.

In pregnancies of a normal birthweight ratio the risks of late fetal death were influenced by maternal age, smoking habits, multiple births, and severe pre-eclampsia. These factors increase the risks of severe placental complications,15-18 which may cause fetal death without affecting the birthweight ratio.

Late fetal death rates were higher among women older than 35 years regardless of the birthweight ratio. The risk of late fetal death has been reported to increase progressively with gestational age and this increase is pronounced among women older than 35 years. 19 20 Risks of placental complications increase with maternal age, and vascular degenerative changes have been observed in the uterine and myometrial arteries of women of older childbearing age 21 22 ; this suggests that late fetal death may be due to an age related effect as a consequence of uteroplacental underperfusion.

Methodological considerations
Chance is an unlikely explanation for our findings because of the large size of the study and the correspondingly narrow confidence intervals of our observed rates and odds ratios. The prospective nature of data collection precludes recall bias. As some risk factors of a fetus being small for gestational age are associated with increased risks of congenital anomalies the study was restricted to pregnancies without congenital malformations.

The conclusions from this investigation are, however, limited by the risk factors included in the birth register. We lacked information on the womens' socioeconomic position, prepregnancy body mass index, and weight gain during pregnancy, which are important determinants of birthweight ratio.1 Socioeconomic position and prepregnancy body mass index are also associated with the risk of late fetal death. 23 24 The association between weight gain during pregnancy and late fetal death, however, is less certain. 24 25 The risks of a fetus being small for gestational age and late fetal death related to maternal age and smoking habits, however, seem to be largely independent of socioeconomic position and prepregnancy body mass index. 1 23 24 26 Maternal height was not an important factor in the overall risk of late fetal death, which agrees with a previous investigation.24 The effect of maternal height on birthweight ratio is reported to be the same both before and after adjusting for confounders. The effect of maternal height on the risk of late fetal death associated with birthweight ratio is therefore unlikely to be due to residual confounding. 27 28

An accurate estimation of the birthweight ratio in cases of late fetal death is limited as estimates of gestational age and fetal weight are based on time of delivery rather than time of death. This not only leads to an overestimation of gestational age but the dead fetus may also have lost weight before delivery,29 and the birthweight ratio may therefore be underestimated in these pregnancies. The extent of this bias is, however, probably limited. Firstly, almost all pregnant women in Sweden follow the routine schedule of visiting their antenatal clinic every second week from 24 weeks' gestation and weekly from 36 weeks, and fetal heart activity is registered at each visit. Secondly, the women are routinely told to contact their antenatal clinic or obstetric department immediately if there is a decrease in fetal movements. Thirdly, the time from diagnosis of a late fetal death to delivery is generally reported as less than 24 hours.30 These factors should ensure a comparatively short delay between the time of fetal death and the time of delivery. In a study of fetal histology and stillbirth in the United States, it was estimated that 80% of all stillbirths were delivered within one week of death.31

Conclusions
Highlighting the risk factors of late fetal death in small for gestational age fetuses is especially important in countries with low infant mortality rates. In the present study, in which all infants with congenital malformations were excluded, late fetal deaths accounted for more than 50% of all late fetal and infant deaths in Sweden from 1983 to 1992. This study shows that the risk of late fetal death in a small for gestational age fetus may be modified by the underlying determinants of birthweight ratio. The very strong relation between late fetal death and a small for gestational age fetus should, however, be re-emphasised; a fetus that is extremely small for gestational age is associated with a high risk of late fetal death, regardless of cause, and must therefore be monitored.

    Acknowledgments

Dr Kramer is a distinguished scientist of the Medical Research Council of Canada.

Contributors: SC participated in the discussion of the study hypothesis and study design, contributed to the analyses, and was mainly responsible for writing the paper; he will act as guarantor of the paper. BH participated in the discussion of the study hypothesis and study design, performed the analyses, and contributed to writing the paper. MSK initiated the study, participated in the discussions of the study hypothesis and study design, contributed to the analyses, and helped write the paper.
    References
Top
Abstract
Introduction
Subjects and methods
Results
Discussion
References

  1. Kramer S. Intrauterine growth and gestational duration determinants. Pediatrics 1987; 80: 502-511[Abstract/Free Full Text].
  2. Khoury MJ, Ericson JD, Cordero JF, McCarthy BJ. Congenital malformations and intrauterine growth retardation: a population study. Pediatrics 1988; 82: 83-90[Abstract/Free Full Text].
  3. Ounstedt M, Moar V, Scott A. Perinatal morbidity and mortality in small-for-dates babies: the relative contribution of some maternal factors. Early Hum Dev 1981; 5: 367-375[Medline].
  4. Snijders RJM, Sherrod C, Gosden CM, Nicolaides KH. Fetal growth retardation: associated malformations and chromosomal abnormalities. Am J Obstet Gynecol 1993; 168: 547-555[Medline].
  5. Heinrich UE. Intrauterine growth retardation and familial short stature. Clin Endocrinol Metab 1992; 6: 589-601.
  6. Wennergren M. Antenatal screening and risk factors for intrauterine growth retardation. Int J Tech Assess Health Care 1992; 8(suppl 1): 147-151.
  7. Gardosi J, Chang A, Kalyan B, Sahota D, Symonds EM. Customised antenatal growth. Lancet 1992; 339: 283-287[Medline].
  8. Sanderson DA, Wilcox MA, Johnson IR. The individualised birthweight ratio: a new method of identifying intrauterine growth retardation. Br J Obstet Gynaecol 1994; 101: 310-314[Medline].
  9. Kramer MS, Oliver M, McLean FH, Dougherty GE, Willis DM, Usher RH. Determinants of fetal growth and body proportionality. Pediatrics 1990; 86: 18-26[Abstract/Free Full Text].
  10. Sciscione AC, Gorman R, Callan NA. Adjustment of birth weight standards for maternal and infant characteristics improves the prediction of outcome in the small-for-gestational-age infant. Am J Obstet Gynecol 1996; 175: 544-547[Medline].
  11. Cnattingius S, Ericson A, Gunnarskog J, Källén B. A quality study of a medical birth registry. Scand J Social Med 1990; 18: 143-148[Medline].
  12. National High Blood Pressure Education Program Working Group on high blood pressure in pregnancy. Am J Obstet Gynecol 1990; 163: 1689-1712.
  13. Högberg U, Larsson N. Early dating by ultrasound and perinatal outcome---a cohort study. Acta Obstet Gynecol Scand 1997; 76: 907-912[Medline].
  14. Åberg A, Lindmark G. Competence and compliance in antenatal care. Experience from Sweden. Int J Tech Assess Health Care 1992; 8(suppl 1): 20-24.
  15. Abdella TN, Sibai BM, Hays JM, Anderson GD. Relationship of hypertensive disease to abruptio placentae. Obstet Gynecol 1984; 63: 365-370[Abstract/Free Full Text].
  16. Cnattingius S. Maternal age modifies the effect of maternal smoking on intrauterine growth retardation but not on late fetal death and placental abruption. Am J Epidemiol 1997; 145: 319-323[Abstract/Free Full Text].
  17. Naeye RL. The duration of maternal cigarette smoking, fetal and placental disorders. Early Hum Dev 1979; 3: 229-237[Medline].
  18. Raymond EG, Mills JL. Placental abruption. Maternal risk factors and associated fetal conditions. Acta Obstet Gynecol Scand 1993; 72: 633-639[Medline].
  19. Raymond EG, Cnattingius S, Kiely JL. Effects of maternal age, parity and smoking on the risk of stillbirth. Br J Obstet Gynaecol 1994; 101: 301-306[Medline].
  20. Yudkin PL, Wood L, Redman CWG. Risk of unexplained stillbirth at different gestational ages. Lancet 1987; i: 1192-1194.
  21. Cnattingius S, Larsson E, Weiner E. Uterine-arterial changes with age and smoking. Int J Feto-Maternal Med 1990; 3: 15-18.
  22. Naeye RL. Maternal age, obstetric complications, and the outcome of pregnancy. Obstet Gynecol 1983; 61: 210-216[Abstract/Free Full Text].
  23. Cnattingius S, Bergström R, Lipworth L, Kramer MS. Prepregnancy weight and the risk of adverse pregnancy outcomes. N Engl J Med 1998; 338: 147-152[Abstract/Free Full Text].
  24. Little RE, Weinberg CR. Risk factors for antepartum and intrapartum stillbirth. Am J Epidemiol 1993; 137: 1177-1189[Abstract/Free Full Text].
  25. Rydhström H, Tydén T, Herbst A, Ljugblad U, Walles B. No relation between maternal weight gain and stillbirth. Acta Obstet Gynecol Scand 1994; 73: 779-781[Medline].
  26. Haglund B, Cnattingius S, Nordström M-L. Social differences in late fetal death and infant mortality in Sweden 1985-86. Pediatr Perinatal Epidemiol 1993; 7: 33-44.[Medline]
  27. Barros FC, Huttly SRA, Victora CG, Kirkwood BR, Vaughan JP. Comparison of the causes and consequences of prematurity and intrauterine growth retardation: a longitudinal study in southern Brazil. Pediatrics 1992; 90: 238-244[Abstract/Free Full Text].
  28. Lang JM, Lieberman E, Cohen A. A comparision of risk factors for preterm labor and term small-for-gestational-age birth. Epidemiology 1996; 7: 369-376[Medline].
  29. Alessandri LM, Stanley FJ, Garner JB, Newnham J, Walters BNJ. A case-control study of unexplained antepartum stillbirths. Br J Obstet Gynaecol 1992; 99: 711-718[Medline].
  30. Rådestad I, Steineck G, Nordin C, Sjögren C. Psychological complications after stillbirth---influence of memories and immediate management: population based study. BMJ 1996; 312: 1505-1508[Abstract/Free Full Text].
  31. Genest DR, Williams MA, Greene MF. Estimating the time of death in stillborn fetuses: I. Histologic evaluation of fetal organs; an autopsy study of 150 stillborn. Obstet Gynecol 1992; 80: 575-584[Abstract/Free Full Text].

(Accepted 4 February 1998)


© BMJ 1998

Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?

Relevant Article

Some small for gestational age fetuses have higher risk of late fetal death than others
BMJ 1998 316: 0. [Full Text]

This article has been cited by other articles:

  • Bukowski, R., Uchida, T., Smith, G. C. S., Malone, F. D., Ball, R. H., Nyberg, D. A., Comstock, C. H., Hankins, G. D. V., Berkowitz, R. L., Gross, S. J., Dugoff, L., Craigo, S. D., Timor, I. E., Carr, S. R., Wolfe, H. M., D'Alton, M. E., for the First and Second Trimester Evaluation of R, (2008). Individualized Norms of Optimal Fetal Growth: Fetal Growth Potential. Obstet Gynecol 111: 1065-1076 [Abstract] [Full text]  
  • Cripe, S. M., Phung, T. T. T., Nguyen, T. P. L., Williams, M. A. (2007). Risk Factors Associated with Stillbirth in Thai Nguyen Province, Vietnam. J Trop Pediatr 53: 366-367 [Abstract] [Full text]  
  • Tita, A. T. N., Salihu, H. M., Ramsey, P. S. (2006). Impact of Anomalous Triplets on Morbidity Outcomes of Normal In Utero Siblings.. Obstet Gynecol 107: 1352-1356 [Abstract] [Full text]  
  • Getahun, D., Ananth, C. V., Selvam, N., Demissie, K. (2005). Adverse Perinatal Outcomes Among Interracial Couples in the United States. Obstet Gynecol 106: 81-88 [Abstract] [Full text]  
  • Regidor, E, Ronda, E, Garcia, A M, Dominguez, V (2004). Paternal exposure to agricultural pesticides and cause specific fetal death. Occup. Environ. Med. 61: 334-339 [Abstract] [Full text]  
  • Surkan, P. J., Stephansson, O., Dickman, P. W., Cnattingius, S. (2004). Previous Preterm and Small-for-Gestational-Age Births and the Subsequent Risk of Stillbirth. NEJM 350: 777-785 [Abstract] [Full text]  
  • Vestergaard, M, Basso, O, Henriksen, T B, Ostergaard, J, Secher, N J, Olsen, J (2003). Pre-eclampsia and febrile convulsions. Arch. Dis. Child. 88: 726-727 [Abstract] [Full text]  
  • Smith, G. C. S., Pell, J. P., Dobbie, R. (2003). Risk of Sudden Infant Death Syndrome and Week of Gestation of Term Birth. Pediatrics 111: 1367-1371 [Abstract] [Full text]  
  • Ananth, C. V., Demissie, K., Kramer, M. S., Vintzileos, A. M. (2003). Small-for-Gestational-Age Births Among Black and White Women: Temporal Trends in the United States. Am. J. Public Health 93: 577-579 [Full text]  
  • Odegard, R. A., Vatten, L. J., Nilsen, S. T., Salvesen, K. A., Vefring, H., Austgulen, R. (2001). Umbilical Cord Plasma Interleukin-6 and Fetal Growth Restriction in Preeclampsia: A Prospective Study in Norway. Obstet Gynecol 98: 289-294 [Abstract] [Full text]  
  • Goodlin, R. C., Odegard, R. (2001). PREECLAMPSIA AND FETAL GROWTH. Obstet Gynecol 97: 640-640 [Full text]  
  • Stephansson, O., Dickman, P. W., Johansson, A., Cnattingius, S. (2000). Maternal Hemoglobin Concentration During Pregnancy and Risk of Stillbirth. JAMA 284: 2611-2617 [Abstract] [Full text]  
  • Ferrer, R. L., Sibai, B. M., Mulrow, C. D., Chiquette, E., Stevens, K. R., Cornell, J. (2000). MANAGEMENT OF MILD CHRONIC HYPERTENSION DURING PREGNANCY: A REVIEW. Obstet Gynecol 96: 849-860 [Abstract] [Full text]  
  • Martinelli, I., Taioli, E., Cetin, I., Marinoni, A., Gerosa, S., Villa, M. V., Bozzo, M., Mannucci, P. M. (2000). Mutations in Coagulation Factors in Women with Unexplained Late Fetal Loss. NEJM 343: 1015-1018 [Abstract] [Full text]  
  • Ekbom, A., Wuu, J., Adami, H.-O., Lu, C.-M., Lagiou, P., Trichopoulos, D., Hsieh, C.-c. (2000). Duration of Gestation and Prostate Cancer Risk in Offspring. Cancer Epidemiol. Biomarkers Prev. 9: 221-223 [Abstract] [Full text]  
  • Kramer, M. S., Platt, R., MSc, H. Y., McNamara, H., Usher, R. H. (1999). Are All Growth-restricted Newborns Created Equal(ly)?. Pediatrics 103: 599-602 [Abstract] [Full text]  



Access all current jobs at BMJ Group
Whats new online at Student 

BMJ
Listen to the latest 

BMJ Interview