Report of a black South African child with oculodentodigital dysplasia and a novel GJA1 gene mutation

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	American journal of medical genetics. Part A 2008-05, Vol.146A (10), p.1350-1353
Hauptverfasser:	Feller, Liviu, Wood, Neil H., Sluiter, Michelle D., Noffke, Claudia, Raubenheimer, Erich J., Lemmer, Johan, van Rensburg, Elizabeth J.
Format:	Artikel
Sprache:	eng
Schlagworte:	African Continental Ancestry Group - genetics Biological and medical sciences Child Connexin 43 - genetics Craniofacial Abnormalities - genetics Diseases of the osteoarticular system Eye Abnormalities - genetics Eye Abnormalities - physiopathology Fingers - abnormalities Humans Male Malformations and congenital and or hereditary diseases involving bones. Joint deformations Medical genetics Medical sciences Mutation Odontodysplasia - genetics Odontodysplasia - physiopathology South Africa Syndactyly Syndrome Tooth Abnormalities - genetics
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!