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Journal De Genetique Humaine|December 1, 1988
[Holoprosencephaly, polydactyly, cardiopathy: new syndrome or a new case of hydrolethalus?]S A André, M P Cordier, A M Beaufrère, et al.Journal De Genetique Humaine|December 1, 1988
[A case of terminal renal insufficiency revealing a "charge" association in an adult]E Renoult, D Sirbat, M KesslerJournal De Genetique Humaine|December 1, 1988
[Chondrodysplasia punctata. Report of four cases in two sibships]P Parent, A Le Gonidec, H Le Guern, et al.Journal De Genetique Humaine|October 1, 1979
[Segregation of HLA haplotypes in a family with infants having spina bifida]S Kulakowski, M Delire, M De BruyereJournal De Genetique Humaine|August 1, 1987
[Congenital stenosis of the aqueduct of Sylvius transmitted in an autosomal recessive mode (5 cases in 2 families)]P Vanlieferinghen, J Chazal, C Francannet, et al.Journal De Genetique Humaine|August 1, 1986
[Hereditary multicentric osteolysis]M C Addor, G Pescia, D Egloff, et al.Journal De Genetique Humaine|August 1, 1986
[Incidence of occult lumbro-sacral spina bifida in parents of children with spina bifida (concerning 80 pairs of parents with affected children)]A Carsin, H Journel, M Roussey, et al.Journal De Genetique Humaine|June 1, 1985
[Apropos of the molecular biology of Huntington's chorea]J Frézal, M L Briard, J KaplanJournal De Genetique Humaine|January 1, 1988
[Chromosome X-linked mental retardation and marfanoid syndrome]J P Fryns, M Buttiens, H van den BergheJournal De Genetique Humaine|January 1, 1988
[t(Y; 15) translocation in a fertile male, detected at the time of amniocentesis]M F Berthéas, D Germain, B Lauras, et al.Pageof 47