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Journal De Genetique Humaine|November 1, 1986
[A case of congenital non-spherocytic hemolytic anemia caused by enzyme deficiency in pyruvate kinase]M Clavier, P Parent, Y Castel, et al.Journal De Genetique Humaine|November 1, 1986
[A case of congenital non-spherocytic hemolytic anemia caused by triose phosphate isomerase deficiency. Prenatal diagnosis]J Poinsot, P Parent, D Alix, et al.Journal De Genetique Humaine|December 1, 1985
[Familial adrenoleukodystrophy]J M Le Fur, F Le Meur, P Parent, et al.Pediatrie|January 1, 1987
[Apropos of a familial case of adrenoleukodystrophy related to X chromosome diagnosed prenatally]P Parent, F Le Meur, D Alix, et al.Journal 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.Annales De Genetique|March 1, 1976
[Partial trisomy 15q due to maternal translocation t(7;15)(q35;14)]Y Castel, D Rivière, J Y Boycly, et al.Archives Francaises De Pediatrie|April 1, 1982
[XXXXY syndrome]L Toudic, G L'Henoret, D Rivière, et al.Journal De Genetique Humaine|November 1, 1982
[Postaxial polydactyly in a female neonate associated with hydrocolpos due to vaginal atresia and with a congenital cardiopathy: the McKusick-Kaufman syndrome]Y Castel, L Toudic, D Alix, et al.Pediatrie|June 1, 1983
[Association of trisomy 21 and gonosomal trisomy. Apropos of 2 cases]Y Castel, B Le Marec, L Toudic, et al.Journal De Genetique Humaine|September 1, 1983
[Clinical evolution and cytogenetic study of two acute lymphoblastic leukemia (type L2) in the child: prognostic value of the karyotype]Y Castel, D Rivière, L Toudic, et al.Pageof 43