Showing results (11-20 of 137) with videos related to
Sort By:
Pageof 14
Archives Francaises De Pediatrie|May 1, 1979
[Acanthosis nigricans, hirsutism and insulin-resistant diabetes]M Colle, P Doyard, J L Chaussain, et al.Annales De Genetique|September 1, 1977
[Partial trisomy 13 due to maternal translocation t(2;13)]F Giraud, J F Mattei, M G MatteiHuman Genetics|January 1, 1984
Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysisM G Mattei, N Souiah, J F MatteiHuman Genetics|January 1, 1983
Prader-Willi syndrome and chromosome 15. A clinical discussion of 20 casesJ F Mattei, M G Mattei, F GiraudArchives Francaises De Pediatrie|August 1, 1985
[Contribution of in situ hybridization to chromosomal analysis]M G Mattei, J F Mattei, F GiraudJournal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1981
[45X/46XY/46XrY mosaic with banding and the Turner phenotype (author's transl)]L Aubert, C Verdet, F Giraud, et al.Pediatrie|January 1, 1992
[Fragile X syndrome: current knowledge]M C Pellissier, M A Voelckel, J F MatteiArchives Francaises De Pediatrie|January 1, 1976
[Humoral immunity and blastic transformation of lymphocytes in trisomy 21]R Bernard, S Sitrk, D Bernard, et al.La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|April 18, 1979
[Asymetrical gonadal dysgenesis. Report of a case (author's transl)]P Chapoy, J F Mattei, C Exbrayat, et al.Annales De Genetique|January 1, 1979
[Asymmetrical gonadal dysgenesis. Report of a case (author's transl)]P Chapoy, J F Mattei, C Exbrayat, et al.Pageof 14