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Nature Genetics|May 1, 1996
Localization of the gene for Cowden disease to chromosome 10q22-23M R Nelen, G W Padberg, E A Peeters, et al.Journal of Medical Genetics|October 28, 2010
A clinical and molecular genetic study of 112 Iranian families with primary microcephalyH Darvish, S Esmaeeli-Nieh, G B Monajemi, et al.Molecular Psychiatry|August 24, 2016
De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and femalesE E Palmer, T Stuhlmann, S Weinert, et al.Molecular Psychiatry|February 4, 2015
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genesH Hu, S A Haas, J Chelly, et al.Pageof 21