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Journal De Genetique Humaine|December 1, 1985
[Prenatal diagnosis of triploidy. II. Biological studies]S Gilgenkrantz, P Mujica, P Perrier, et al.Journal De Genetique Humaine|January 1, 1988
[Robertsonian translocation and genetic counseling]L F Formiga, B Le Marec, F Serville, et al.La Nouvelle Presse Medicale|January 17, 1976
[XXYY chromosomal constitution recognised during the 1st year of life]S Gilgenkrantz, G Mauuary, M Saborio, et al.Annales De Genetique|January 1, 1989
A case of Alagille's syndrome with translocation (4;14) (q21;q21)P Mujica, A Morali, M Vidailhet, et al.Journal De Genetique Humaine|March 1, 1983
[Chromosome 11 and cancer]M J Gregoire, C Pernot, F Himont, et al.Nature|October 13, 1983
c-Ha-ras1 is not deleted in aniridia-Wilms' tumour associationC Huerre, S Despoisse, S Gilgenkrantz, et al.Human Genetics|February 1, 1996
X chromosome inactivation in 30 girls with Rett syndrome: analysis using the probeP Camus, N Abbadi, M C Perrier, et al.Pediatrie|January 1, 1989
[Noonan's syndrome and its cardiovascular dysplasia. Apropos of 64 cases]C Pernot, A M Worms, F Marçon, et al.Journal De Genetique Humaine|January 1, 1989
[Clinical and biological studies of 14 cases of the Prader-Labhart-Willi syndrome]P Mujica, B Leheup, S Gilgenkrantz, 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.Pageof 24