Non-invasive prenatal diagnosis of single-gene disorders from maternal blood-Reference-Cited by-同舟云学术

Non-invasive prenatal diagnosis of single-gene disorders from maternal blood

Published:2012-08 Issue:1 Volume:504 Page:144-149
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Bustamante-Aragonés Ana,Rodríguez de Alba Marta,Perlado Sara,Trujillo-Tiebas María José,Arranz Javier Plaza,Díaz-Recasens Joaquín,Troyano-Luque Juan,Ramos Carmen

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference47 articles.

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4. Foetal sex determination in maternal blood from the seventh week of gestation and its role in diagnosing haemophilia in the foetuses of female carriers;Bustamante-Aragones;Haemophilia,2008

5. New strategy for the prenatal detection/exclusion of paternal cystic fibrosis mutations in maternal plasma;Bustamante-Aragones;J. Cyst. Fibros.,2008

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