An urgent need for a change in policy revealed by a study on prenatal testing for Duchenne muscular dystrophy-Reference-Cited by-同舟云学术

An urgent need for a change in policy revealed by a study on prenatal testing for Duchenne muscular dystrophy

Published:2012-06-06 Issue:1 Volume:21 Page:21-26
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Helderman-van den Enden Apollonia T J M,Madan Kamlesh,Breuning Martijn H,van der Hout Annemieke H,Bakker Egbert,de Die-Smulders Christine E M,Ginjaar Hendrika B

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/ejhg2012101.pdf

Reference29 articles.

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4. Bakker E, Hofker MH, Goor N et al. Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs. Lancet 1985; 1: 655–658.

5. de Die-Smulders CE, Geraedts JP, Dreesen JC, Coonen E, Land JA : Genetic diagnosis of IVF embryos: preliminary results from ‘preimplantation genetic diagnoses’ in the Netherlands. Ned Tijdschr Geneeskd 1998; 142: 2441–2444.

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