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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|September 1, 1989
[Balanced X-autosomal translocation and mental retardation. Mapping mental retardation linked to X (excluding fragile X)]M Teboul, P Mujica, M Chery, 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.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|January 1, 1989
[Clinical and biological studies of 14 cases of the Prader-Labhart-Willi syndrome]P Mujica, B Leheup, S Gilgenkrantz, et al.Human Genetics|January 1, 1989
Hypohidrotic ectodermal dysplasia. Clinical study of a family of 30 over three generationsS Gilgenkrantz, C Blanchet-Bardon, V Nazzaro, et al.Journal De Genetique Humaine|August 1, 1986
[Unexpected chromosomal abnormalities in prenatal diagnosis. 4 case reports with preservation of the pregnancy]S Gilgenkrantz, M Schweitzer, P Droulle, et al.Genomics|July 1, 1993
Physical mapping of DNA markers in the q13-q22 region of the human X chromosomeC Philippe, F P Cremers, M Chery, et al.Annales De Genetique|January 1, 1989
Interstitial deletion of the long arm of chromosome 6M Chery, L F Formiga, P Mujica, et al.Oncogene|July 1, 1990
Sublocalisation of the X breakpoint in the translocation (X; 18)(p11.2; q11.2) primary change in synovial sarcomasS Gilgenkrantz, M Chery, M Teboul, et al.Pageof 10