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Browsing by Author Weil, D

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	Title	Author(s)	Issue Date
	A base substitution in the exon of a collagen gene causes alternative splicing and generates a structurally abnormal polypeptide in a patient with Ehlers-Danlos Syndrome Type VII Journal:EMBO Journal	Weil, D D'alessio, M Ramirez, F De Wet, W Cole, WG Chan, D Bateman, JF	1989
	Connexin 26 gene linked to a dominant deafness [9] Journal:Nature	Denoyelle, F LinaGranade, G Plauchu, H Bruzzone, R Chaib, H Levi Acobas, F Weil, D Petit, C	1998
	Functional analysis of a dominant mutation of human connexin26 associated with nonsyndromic deafness Journal:Cell Communication and Adhesion	Bruzzone, R Gomès, D Denoyelle, F Duval, N Perea, J Veronesi, V Weil, D Petit, C Gabellec, MM D'Andrea, P White, TW	2001

Showing results 1 to 3 of 3