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D Weil

Showing results (201-210 of 203) with videos related to

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Human Molecular Genetics|October 23, 1997
Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 geneF Denoyelle, D Weil, M A Maw, et al.
Journal of Medical Genetics|July 5, 2005
A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairmentF J del Castillo, M Rodríguez-Ballesteros, A Alvarez, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 22, 2015
[Does prenatal diagnosis modify neonatal management and early outcome of children with esophageal atresia type III?]C Garabedian, R Sfeir, C Langlois, et al.
Pageof 21

Showing results (201-210 of 203) with videos related to

Sort By:
Pageof 21
You have reached the last page of results.This site can display upto 203 results.
Human Molecular Genetics|October 23, 1997
Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 geneF Denoyelle, D Weil, M A Maw, et al.
Journal of Medical Genetics|July 5, 2005
A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairmentF J del Castillo, M Rodríguez-Ballesteros, A Alvarez, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 22, 2015
[Does prenatal diagnosis modify neonatal management and early outcome of children with esophageal atresia type III?]C Garabedian, R Sfeir, C Langlois, et al.
Pageof 21