Services for people with haemoglobinopathyBMJ 1994; 308 doi: https://doi.org/10.1136/bmj.308.6945.1714 (Published 25 June 1994) Cite this as: BMJ 1994;308:1714
- L Luzzato
- Hammersmith Hospital, London W12 0NN
EDITOR, - Sally Davies has expressed her concern, which I share, on the quality and quantity of services available to patients with sickle cell anaemia, as compared with those available to patients with other inherited disorders.1 I find it pertinent to note how much population genetics can affect public health.
With a heterozygote (AS) …
Log in using your username and password
Log in through your institution
Register for a free trial to thebmj.com to receive unlimited access to all content on thebmj.com for 14 days.
Sign up for a free trial