Pseudotrisomy 13 and autosomal recessive holoprosencephaly.

Two sibs, diagnosed prenatally, had holoprosencephaly, midface hypoplasia, and normal chromosomes. The first fetus also had polydactyly. This sibship may represent an example of autosomal recessive pseudotrisomy 13.

Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Seller, M J, Chitty, L S, Dunbar, H
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1993
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1016613/
https://ncbi.nlm.nih.gov/pubmed/8301659
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller