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Journal De Genetique Humaine|December 1, 1981
[Association, in the same subject, of deletion of the short arm of chromosome 4 (4p-) and of complete deficiency of parahydroxyphenyl-pyruvate oxidase activity in the liver (tyrosinosis)]G Malpuech, J F Mattei, J Gaulme, et al.Journal of Mental Deficiency Research|September 1, 1979
Erythrocyte copper levels in children with trisomy 21B Mallet, P Poulet, S Ayme, et al.Human Genetics|January 1, 1987
Monosomy 21: a new case confirmed by in situ hybridizationM C Pellissier, N Philip, M A Voelckel-Baeteman, et al.Human Genetics|December 1, 1988
Dissociation between mental retardation and fragile site expression in a family with fragile X-linked mental retardationM A Voelckel, M G Mattei, C N'Guyen, et al.Pediatrie|January 1, 1992
[Vitamin D-resistant rickets type II: apropos of 2 cases]G Simonin, B Chabrol, E Moulene, et al.Human Genetics|November 1, 1988
The gene encoding the large human neurofilament subunit (NF-H) maps to the q121-q131 region on human chromosome 22M G Mattei, A Dautigny, D Pham-Dinh, et al.Human Genetics|October 1, 1988
Assignment of the human hap retinoic acid receptor RAR beta gene to the p24 band of chromosome 3M G Mattei, H de Thé, J F Mattei, et al.Archives Francaises De Pediatrie|December 1, 1977
[Clouston's ectodermal dysplasia. A case report with biochemical study of keratin]F Giraud, J F Mattei, M Rolland, et al.Annales D'Endocrinologie|January 1, 1977
[Apparent internal male pseudo-hermaphroditism. Gynecomastia. Negative gonad surgical research. Caryotype 46, XX. Presence of H-Y antigen (author's transl)]J Vague, J Guidon, J F Mattei, et al.Human Genetics|November 1, 1988
Trisomy 21q223 and Down's phenotype correlation evidenced by in situ hybridizationM C Pellissier, M Laffage, N Philip, et al.Pageof 14