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L Al-Gazali

Showing results (21-30 of 26) with videos related to

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American Journal of Human Genetics|July 11, 2006
Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndromeC G Woods, S Stricker, P Seemann, et al.
Clinical Genetics|February 2, 2018
Expanding the clinical and genetic spectra of NKX6-2-related disorderC Baldi, A M Bertoli-Avella, N Al-Sannaa, et al.
Neurology|January 26, 2011
Distinguishing 3 classes of corpus callosal abnormalities in consanguineous familiesR M Hanna, S E Marsh, D Swistun, et al.
Clinical Genetics|February 24, 2017
Chondrodysplasia with multiple dislocations: comprehensive study of a series of 30 casesE Ranza, C Huber, N Levin, et al.
Molecular Syndromology|May 9, 2013
Evaluation of Clinical Manifestations in Patients with Severe Lymphedema with and without CCBE1 MutationsM Alders, A Mendola, L Adès, 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 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
American Journal of Human Genetics|July 11, 2006
Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndromeC G Woods, S Stricker, P Seemann, et al.
Clinical Genetics|February 2, 2018
Expanding the clinical and genetic spectra of NKX6-2-related disorderC Baldi, A M Bertoli-Avella, N Al-Sannaa, et al.
Neurology|January 26, 2011
Distinguishing 3 classes of corpus callosal abnormalities in consanguineous familiesR M Hanna, S E Marsh, D Swistun, et al.
Clinical Genetics|February 24, 2017
Chondrodysplasia with multiple dislocations: comprehensive study of a series of 30 casesE Ranza, C Huber, N Levin, et al.
Molecular Syndromology|May 9, 2013
Evaluation of Clinical Manifestations in Patients with Severe Lymphedema with and without CCBE1 MutationsM Alders, A Mendola, L Adès, 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 3