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C Moraine

Showing results (51-60 of 94) with videos related to

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European Journal of Human Genetics : EJHG|June 15, 2000
Systematic analysis of X-inactivation in 19XLMR families: extremely skewed profiles in carriers in three familiesM Raynaud, M P Moizard, B Dessay, et al.
American Journal of Medical Genetics|April 6, 1999
Evidence for a new X-linked mental retardation gene in Xp21-Xp22: clinical and molecular data in one familyN Ronce, M Raynaud, A Toutain, et al.
European Journal of Human Genetics : EJHG|July 26, 2000
Severe cognitive impairment in DMD: obvious clinical indication for Dp71 isoform point mutation screeningM P Moizard, A Toutain, D Fournier, et al.
American Journal of Medical Genetics|January 30, 1995
Lumping Juberg-Marsidi syndrome and X-linked alpha-thalassemia/mental retardation syndrome?P Saugier-Veber, A Munnich, S Lyonnet, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1997
Deafness and Mondini dysplasia in Kabuki (Niikawa-Kuroki) syndrome. Report of a case and review of the literatureA Toutain, Y Plée, M J Ployet, et al.
American Journal of Medical Genetics|September 24, 1999
Splenogonadal fusion limb defect syndrome: report of five new cases and reviewD Bonneau, J Roume, M Gonzalez, et al.
Cancer Genetics and Cytogenetics|June 1, 1992
Structural rearrangements of chromosome 13 as additional abnormalities in Burkitt lymphoma and type 3 acute lymphoblastic leukemiaC Barin, C Valtat, S Briault, et al.
American Journal of Medical Genetics|October 26, 2000
Exclusion of nine candidate genes for their involvement in X-linked FG syndrome (FGS1) in three familiesA M Lossi, L Colleaux, P Chiaroni, et al.
Revue Francaise De Gynecologie Et D'Obstetrique|October 1, 1984
[Should we still explore placental sulfatase deficiencies? Reflections apropos of a case report]Y Giovangrandi, G Magnin, E Sauvanet, et al.
Human Genetics|February 1, 1997
Nance-Horan syndrome: linkage analysis in 4 families refines localization in Xp22.31-p22.13 regionA Toutain, N Ronce, B Dessay, et al.
Pageof 10

Showing results (51-60 of 94) with videos related to

Sort By:
Pageof 10
European Journal of Human Genetics : EJHG|June 15, 2000
Systematic analysis of X-inactivation in 19XLMR families: extremely skewed profiles in carriers in three familiesM Raynaud, M P Moizard, B Dessay, et al.
American Journal of Medical Genetics|April 6, 1999
Evidence for a new X-linked mental retardation gene in Xp21-Xp22: clinical and molecular data in one familyN Ronce, M Raynaud, A Toutain, et al.
European Journal of Human Genetics : EJHG|July 26, 2000
Severe cognitive impairment in DMD: obvious clinical indication for Dp71 isoform point mutation screeningM P Moizard, A Toutain, D Fournier, et al.
American Journal of Medical Genetics|January 30, 1995
Lumping Juberg-Marsidi syndrome and X-linked alpha-thalassemia/mental retardation syndrome?P Saugier-Veber, A Munnich, S Lyonnet, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1997
Deafness and Mondini dysplasia in Kabuki (Niikawa-Kuroki) syndrome. Report of a case and review of the literatureA Toutain, Y Plée, M J Ployet, et al.
American Journal of Medical Genetics|September 24, 1999
Splenogonadal fusion limb defect syndrome: report of five new cases and reviewD Bonneau, J Roume, M Gonzalez, et al.
Cancer Genetics and Cytogenetics|June 1, 1992
Structural rearrangements of chromosome 13 as additional abnormalities in Burkitt lymphoma and type 3 acute lymphoblastic leukemiaC Barin, C Valtat, S Briault, et al.
American Journal of Medical Genetics|October 26, 2000
Exclusion of nine candidate genes for their involvement in X-linked FG syndrome (FGS1) in three familiesA M Lossi, L Colleaux, P Chiaroni, et al.
Revue Francaise De Gynecologie Et D'Obstetrique|October 1, 1984
[Should we still explore placental sulfatase deficiencies? Reflections apropos of a case report]Y Giovangrandi, G Magnin, E Sauvanet, et al.
Human Genetics|February 1, 1997
Nance-Horan syndrome: linkage analysis in 4 families refines localization in Xp22.31-p22.13 regionA Toutain, N Ronce, B Dessay, et al.
Pageof 10