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Annales De Gastroenterologie Et D'Hepatologie|November 1, 1993
[Molecular genetics of hemochromatosis]J Y Le Gall, V David, J Yaouanq, et al.Human Molecular Genetics|August 11, 1999
Expression of the Sonic hedgehog (SHH ) gene during early human development and phenotypic expression of new mutations causing holoprosencephalyS Odent, T Atti-Bitach, M Blayau, et al.Human Molecular Genetics|April 4, 2001
Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombinationL Y Brown, S Odent, V David, et al.Journal of Inherited Metabolic Disease|July 17, 2007
Neonatal screening of cystic fibrosis: diagnostic problems with CFTR mild mutationsM Roussey, A Le Bihannic, V Scotet, et al.Human Mutation|August 3, 2000
Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in FranceM Claustres, C Guittard, D Bozon, et al.Journal of Medical Genetics|April 16, 2005
Cleft lip/palate and CDH1/E-cadherin mutations in families with hereditary diffuse gastric cancerT Frebourg, C Oliveira, P Hochain, et al.Pageof 3