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Genetic Counseling (Geneva, Switzerland)|June 6, 2015
A rare mutation in EIF2B4 gene in an epileptic child with vanishing white matter disease: a case reportO Gungor, A K Ozkaya, T Hirfanoglu, et al.Genetic Counseling (Geneva, Switzerland)|June 6, 2015
A familial case of Coffin-Lowry syndrome caused by RPS6KA3 C.898C>T mutation associated with multiple abnormal brain imaging findingsT Tos, M Y Alp, A Aksoy, et al.Genetic Counseling (Geneva, Switzerland)|February 28, 2018
Osteocraniosplenic Syndrome-Hypomineralized Skull with Gracile Long Bones and Splenic Hypoplasia: A Case Report and Literature ReviewS Puvabanditsin, M February, V D Stefano, et al.Genetic Counseling (Geneva, Switzerland)|February 28, 2018
Central nervous system abnormalities and psychomotor retardation in a girl with a 15.4-MB deletion of 14q12→q21.2 and a 550-KB deletion of 18p11.23: microarray delineation of an unbalanced chromosome rearrangement and a literature reviewD Torun, M Arslan, H Akar, et al.Genetic Counseling (Geneva, Switzerland)|February 28, 2018
Distal 13q monosomy and neural tube defectsI W Lurie, I V Novikova, O A Tarletskaya, et al.Genetic Counseling (Geneva, Switzerland)|February 28, 2018
Mitochondrial Neurogastrointestinal Encephalopathy: Clinical, Biochemical and Molecular Study in Three Egyptian PatientsL Selim, R Van Coster, D Mehaney, et al.Genetic Counseling (Geneva, Switzerland)|February 28, 2018
Pathogenic Compound Heterozygous Mutations in a Mexican Mestizo Patient with Niemann-Pick Disease Type BJ Salvador Velarde-Félix, J F Osuna-Ramos, M G Sánchez-Leyva, et al.Genetic Counseling (Geneva, Switzerland)|September 15, 2006
Ectrodactyly, ectodermal dysplasia, macular degeneration syndrome: a further contributionM S Yildirim, T C Ogun, U KamişGenetic Counseling (Geneva, Switzerland)|September 15, 2006
Mosaicism for terminal deletion of 4qG E Utine, D AktasGenetic Counseling (Geneva, Switzerland)|September 15, 2006
Cytogenetic results of amniocentesis materials: incidence of abnormal karyotypes in the Turkish collaborative studyM Yirmibes Karaoguz, F Bal, T Yakut, et al.Pageof 116