A gene locus for branchio-otic syndrome maps to chromosome 14q21.3-q24.3

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Autoria(s): Ruf, R. G.; Berkman, J.; Wolf, M. T. F.; Nurnberg, P.; Gattas, M.; Ruf, E. M.; Hyland, V.; Kromberg, J.; Glass, I.; Macmillan, J.; Otto, E.; Nurnberg, G.; Lucke, B.; Hennies, H. C.; Hildebrandt, F.

Contribuinte(s)	E. R. Maher C. Eng
Data(s)	01/07/2003
Identificador	http://espace.library.uq.edu.au/view/UQ:66700
Idioma(s)	eng
Publicador	BMJ Publishing Group
Palavras-Chave	#Genetics & Heredity #Bor Syndrome #Deafness #Localization #Association #Dysplasia #Linkage #Family #Scores #C1 #321011 Medical Genetics #730107 Inherited diseases (incl. gene therapy)
Tipo	Journal Article