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R Borgatti

Showing results (111-120 of 114) with videos related to

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Annals of Neurology|July 14, 2000
Familial perisylvian polymicrogyria: a new familial syndrome of cortical maldevelopmentM M Guerreiro, E Andermann, R Guerrini, et al.
Annals of Neurology|February 16, 1999
Characterization of mutations in the gene doublecortin in patients with double cortex syndromeJ G Gleeson, S R Minnerath, J W Fox, et al.
Journal of Medical Genetics|January 8, 2008
Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesisB W M van Bon, D A Koolen, R Borgatti, et al.
American Journal of Medical Genetics. Part A|September 19, 2009
Expanding CEP290 mutational spectrum in ciliopathiesLorena Travaglini, Francesco Brancati, Tania Attie-Bitach, et al.
Pageof 12

Showing results (111-120 of 114) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 114 results.
Annals of Neurology|July 14, 2000
Familial perisylvian polymicrogyria: a new familial syndrome of cortical maldevelopmentM M Guerreiro, E Andermann, R Guerrini, et al.
Annals of Neurology|February 16, 1999
Characterization of mutations in the gene doublecortin in patients with double cortex syndromeJ G Gleeson, S R Minnerath, J W Fox, et al.
Journal of Medical Genetics|January 8, 2008
Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesisB W M van Bon, D A Koolen, R Borgatti, et al.
American Journal of Medical Genetics. Part A|September 19, 2009
Expanding CEP290 mutational spectrum in ciliopathiesLorena Travaglini, Francesco Brancati, Tania Attie-Bitach, et al.
Pageof 12