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American Journal of Human Genetics|January 13, 2001
High residual activity of PMM2 in patients' fibroblasts: possible pitfall in the diagnosis of CDG-Ia (phosphomannomutase deficiency)S Grünewald, E Schollen, E Van Schaftingen, et al.Acta Endocrinologica|April 1, 1993
Opposite effects of growth hormone and estrogens on the pregnancy zone protein serum levels in children and adolescentsK Devriendt, G Massa, F de Zegher, et al.American Journal of Medical Genetics|July 12, 1996
Linkage analysis in three families with nonspecific X-linked mental retardationS Claes, X X Gu, E Legius, et al.Current Biology : CB|September 22, 2001
NXF5, a novel member of the nuclear RNA export factor family, is lost in a male patient with a syndromic form of mental retardationL Jun, S Frints, H Duhamel, et al.European Journal of Human Genetics : EJHG|August 10, 1999
Mutational analysis of the Cu/Zn superoxide dismutase gene in 23 familial and 69 sporadic cases of amyotrophic lateral sclerosis in BelgiumT Aguirre, G Matthijs, W Robberecht, et al.Human Mutation|July 23, 2003
Gross rearrangements in the MECP2 gene in three patients with Rett syndrome: implications for routine diagnosis of Rett syndromeE Schollen, E Smeets, E Deflem, et al.Journal of Medical Genetics|April 16, 1999
Triplication of distal chromosome 10qK Devriendt, G Matthijs, M Holvoet, et al.Journal of Neuroimmunology|June 1, 1995
Importance of HLA-DRB1 and DQA1 genes and of the amino acid polymorphisms in the functional domain of DR beta 1 chain in multiple sclerosisM Z Ghabanbasani, X X Gu, M Spaepen, et al.Genetic Counseling (Geneva, Switzerland)|April 23, 2005
Medullary thyroid carcinoma in a child with a new RET mutation and a RET polymorphismK Vandenbosch, M Renard, A Uyttebroeck, et al.Clinical Genetics|May 1, 1995
Increased and decreased relative risk for non-insulin-dependent diabetes mellitus conferred by HLA class II and by CD4 allelesM Z Ghabanbasani, M Spaepen, I Buyse, et al.Pageof 28