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Clinical Genetics|December 1, 1989
Evidence for a major additive gene in ulcerative colitisU Monsén, L Iselius, C Johansson, et al.Clinical Genetics|December 1, 1989
Linkage between alpha 1B-glycoprotein (A1BG) and Lutheran (LU) red blood group system: assignment to chromosome 19: new genetic variants of A1BGH Eiberg, M L Bisgaard, J MohrClinical Genetics|December 1, 1989
Achalasia microcephaly syndrome in a patient with consanguineous parents: support for a.m. being a distinct autosomal recessive conditionA Hernández, M C Reynoso, F Soto, et al.Clinical Genetics|June 18, 1998
Glucose-6-phosphatase gene (727G-->T) splicing mutation is prevalent in Hong Kong Chinese patients with glycogen storage disease type 1aC W Lam, W M But, C C Shek, et al.Clinical Genetics|June 18, 1998
Normal growth in Angelman syndrome due to paternal UPDA Smith, L Robson, B BuchholzClinical Genetics|November 1, 1988
Ataxia-without-telangiectasia in two sisters with rearrangements of chromosomes 7 and 14E Maserati, A Ottolini, P Veggiotti, et al.Clinical Genetics|November 1, 1988
Complex chromosome rearrangements involving chromosomes 1;3 and 2;3 in two abnormal childrenL E Voullaire, G C WebbClinical Genetics|April 13, 2020
Further delineation of the female phenotype with KDM5C disease causing variants: 19 new individuals and review of the literatureVirginie Carmignac, Sophie Nambot, Daphné Lehalle, et al.Clinical Genetics|April 13, 2020
Comprehensive molecular analysis of 61 Egyptian families with hereditary nonsyndromic hearing lossBirgit S Budde, Maha Abdelgaber Aly, Mostafa R Mohamed, et al.Clinical Genetics|August 1, 1981
Development of eight pubertal males with 47,xxy karyotypeJ A Salbenblatt, B G Bender, M H Puck, et al.Pageof 719