Significance of heterozygosis M34T mutation of GJB2 gene in non-syndromic congenital deafness. Retrospective analysis of 12,472 samples of amniotic fluid

Significance of heterozygosis M34T mutation of GJB2 gene in non-syndromic congenital deafness. Retrospective analysis of 12,472 samples of amniotic fluid

OBJECTIVE: to determinate the role of heterozygosis of M34T mutation of GJB2 gene in non syndromic congenital deafness

Détails bibliographiques
Publié dans:Journal of prenatal medicine. - 2007. - 7(2013), 4 vom: 20. Okt., Seite 56-8
Auteur principal: Coco, Manuela (Auteur)
Autres auteurs: Salvinelli, Fabrizio, Greco, Fabio, Trivelli, Maurizio, D'Emidio, Laura, Mesoraca, Alvaro, Giorlandino, Claudio, Raffio, Raffaella, Coco, Claudio
Format: Article
Langue:English
Publié: 2013
Accès à la collection:Journal of prenatal medicine
Sujets:Journal Article M34T mutation amniocentesis congenital deafness prenatal diagnosis