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Journal De Genetique Humaine|March 1, 1983
[Chromosome 11 and cancer]M J Gregoire, C Pernot, F Himont, et al.American Journal of Medical Genetics|September 1, 1982
Association of del(11)(p15.1p12), aniridia, catalase deficiency, and cardiomyopathyS Gilgenkrantz, C Vigneron, M J Gregoire, et al.Journal De Genetique Humaine|December 1, 1980
[Phenotype of a ring-chromosome 6 carrier. Clinical and cytogenetic study]F Cruz-Marin, S Gilgenkrantz, M J Gregoire, et al.Journal of Medical Genetics|December 1, 1981
Partial proximal trisomy of the long arm of chromosome 5 (q13 leads to q22) resulting from maternal insertion der ins (10;5)S Gilgenkrantz, P Dulucq, J L Bresson, et al.Bulletin De L'Association Des Anatomistes|June 1, 1976
[Cytogenetic studies in spontaneous abortions]S Gilgenkrantz, M J Gregoire, F StreiffComptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1976
[Action of 5-bromodeoxyuridine as a function of time on the aspect of chromosomes. Attempt at interpretation]S Gilgenkrantz, M J Gregoire, F StreiffArchives Francaises De Pediatrie|November 1, 1975
[Cat eye syndrome with pituitary dwarfism and normal mental development]M Pierson, S Gilgenkrantz, M SaborioHuman Genetics|January 1, 1981
Proximal trisomy 13. A family with balanced reciprocal translocation t(8;13) in seven members and Robertsonian translocation t(13;14) in three membersS Gilgenkrantz, C Defeche, S Stehlin, et al.Journal De Genetique Humaine|March 1, 1976
[Translocation 46,XY,t(2;5) (q37;q14) and mental retardation. Clinical and cytogenetic study]S Gilgenkrantz, R Walbaum, G Mauuary, et al.Journal De Genetique Humaine|July 1, 1984
[Fragile site on chromosome 2 (q11) in a case of familial lymphohistiocytosis]S Gilgenkrantz, M J Gregoire, M Chery, et al.Pageof 37