Showing results (11-20 of 18) with videos related to
Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Case Reports in Genetics|April 30, 2014
Congenital Arthrogryposis: An Extension of the 15q11.2 BP1-BP2 Microdeletion Syndrome?K M Usrey, C A Williams, M Dasouki, et al.Cytogenetics and Cell Genetics|January 1, 1995
Assignment of the gene (GLCLC) that encodes the heavy subunit of gamma-glutamylcysteine synthetase to human chromosome 6E Sierra-Rivera, M L Summar, M Dasouki, et al.Journal of the Neurological Sciences|June 1, 1994
Autosomal recessive ataxia, slow eye movements and psychomotor retardationA S Najim al-Din, A al-Kurdi, M Dasouki, et al.Cytogenetics and Cell Genetics|January 1, 1996
Assignment of the human gene (GLCLR) that encodes the regulatory subunit of gamma-glutamylcysteine synthetase to chromosome 1p21E Sierra-Rivera, M Dasouki, M L Summar, et al.Clinical and Experimental Immunology|July 22, 2020
TREC and KREC profiling as a representative of thymus and bone marrow output in patients with various inborn errors of immunityM Dasouki, A Jabr, G AlDakheel, et al.Pediatric Research|January 3, 2001
Role of common gene variations in the molecular pathogenesis of short-chain acyl-CoA dehydrogenase deficiencyM J Corydon, J Vockley, P Rinaldo, et al.Human Molecular Genetics|July 13, 1999
PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndromeD J Marsh, J B Kum, K L Lunetta, et al.Clinical Genetics|February 17, 2018
Genetic investigation of 93 families with microphthalmia or posterior microphthalmosN Patel, A O Khan, S Alsahli, et al.Pageof 2