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Human Genetics|June 1, 1988
Acquired chromosome rearrangements in human lymphocytes: effect of agingM Prieur, W Al Achkar, A Aurias, et al.Nature Genetics|August 31, 2001
CARD15 mutations in Blau syndromeC Miceli-Richard, S Lesage, M Rybojad, et al.American Journal of Medical Genetics. Supplement|January 1, 1990
Down syndrome critical region around D21S55 on proximal 21q22.3Z Rahmani, J L Blouin, N Créau-Goldberg, et al.Annales De Genetique|March 1, 1977
[Possible localization of the glutathione reductase (EC 1.6.4.2) on the 8p21 band]P M Sinet, J L Bresson, J Couturier, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 28, 2003
[Childhood-onset systemic lupus erythematosus]B Bader-Meunier, P Quartier, G Deschênes, et al.Human Genetics|December 1, 1991
Cytogenetic and molecular analysis of a de novo tandem duplication of chromosome 21J L Blouin, A Aurias, N Créau-Goldberg, et al.American Journal of Medical Genetics|December 5, 2000
Clinical variability and genetic homogeneity of the camptodactyly-arthropathy-coxa vara-pericarditis syndromeL Faivre, A M Prieur, M Le Merrer, et al.Clinical Immunology and Immunopathology|July 1, 1995
Cytokine-mediated bone resorption in patients with the hyperimmunoglobulin E syndromeM Cohen-Solal, A M Prieur, L Prin, et al.The Journal of Pediatrics|January 13, 2005
Long-term survival in severe combined immune deficiency: the role of persistent maternal engraftmentIlhan Tezcan, Fugen Ersoy, Ozden Sanal, et al.European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics|August 24, 1999
Nationwide collaborative study of HLA class II associations with distinct types of juvenile chronic arthritis (JCA) in GreeceP Pratsidou-Gertsi, F Kanakoudi-Tsakalidou, M Spyropoulou, et al.Pageof 19