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  • Mutation screening in British 21-hydroxylase deficiency families and development of novel microsatellite based approaches to prenatal diagnosis

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Original article
Mutation screening in British 21-hydroxylase deficiency families and development of novel microsatellite based approaches to prenatal diagnosis

Authors

  1. Professor Strachan.
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Citation

Lako M, Ramsden S, Campbell RD, et al
Mutation screening in British 21-hydroxylase deficiency families and development of novel microsatellite based approaches to prenatal diagnosis
Journal of Medical Genetics 1999;36:119-124.

Publication history

  • Received March 19, 1998
  • Revised July 2, 1998
  • First published February 1, 1999.
Online issue publication 
April 27, 2016

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Journal of Medical Genetics