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M Fellous

Showing results (231-240 of 246) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|August 6, 1996
Loss of sequences 3' to the testis-determining gene, SRY, including the Y pseudoautosomal boundary associated with partial testicular determinationK McElreavey, E Vilain, S Barbaux, et al.
Nature Genetics|December 17, 1997
Donor splice-site mutations in WT1 are responsible for Frasier syndromeS Barbaux, P Niaudet, M C Gubler, et al.
Journal of Medical Genetics|July 13, 2002
Deletion of 9p associated with gonadal dysfunction in 46,XY but not in 46,XX human fetusesF Vialard, C Ottolenghi, M Gonzales, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 30, 1999
Ullrich-Turner syndrome: relevance of searching for Y chromosome fragmentsD Damiani, D R Guedes, M Fellous, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|March 23, 2001
The brain decade in debate: III. Neurobiology of emotionC Blanchard, R Blanchard, J M Fellous, et al.
Human Reproduction (Oxford, England)|December 1, 2000
Sex chromosome mosaicism in males carrying Y chromosome long arm deletionsJ P Siffroi, C Le Bourhis, C Krausz, et al.
Human Mutation|March 27, 1999
The same mutation affecting the splicing of WT1 gene is present on Frasier syndrome patients with or without Wilms' tumorA S Barbosa, C G Hadjiathanasiou, C Theodoridis, et al.
The Journal of Pathology|March 19, 2008
FOXL2 and SOX9 as parameters of female and male gonadal differentiation in patients with various forms of disorders of sex development (DSD)R Hersmus, N Kalfa, B de Leeuw, et al.
American Journal of Human Genetics|August 27, 1998
Swyer syndrome and 46,XY partial gonadal dysgenesis associated with 9p deletions in the absence of monosomy-9p syndromeR A Veitia, M Nunes, L Quintana-Murci, et al.
Annals of Human Genetics|April 22, 2006
Population structure in the Mediterranean basin: a Y chromosome perspectiveC Capelli, N Redhead, V Romano, et al.
Pageof 25

Showing results (231-240 of 246) with videos related to

Sort By:
Pageof 25
Proceedings of the National Academy of Sciences of the United States of America|August 6, 1996
Loss of sequences 3' to the testis-determining gene, SRY, including the Y pseudoautosomal boundary associated with partial testicular determinationK McElreavey, E Vilain, S Barbaux, et al.
Nature Genetics|December 17, 1997
Donor splice-site mutations in WT1 are responsible for Frasier syndromeS Barbaux, P Niaudet, M C Gubler, et al.
Journal of Medical Genetics|July 13, 2002
Deletion of 9p associated with gonadal dysfunction in 46,XY but not in 46,XX human fetusesF Vialard, C Ottolenghi, M Gonzales, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 30, 1999
Ullrich-Turner syndrome: relevance of searching for Y chromosome fragmentsD Damiani, D R Guedes, M Fellous, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|March 23, 2001
The brain decade in debate: III. Neurobiology of emotionC Blanchard, R Blanchard, J M Fellous, et al.
Human Reproduction (Oxford, England)|December 1, 2000
Sex chromosome mosaicism in males carrying Y chromosome long arm deletionsJ P Siffroi, C Le Bourhis, C Krausz, et al.
Human Mutation|March 27, 1999
The same mutation affecting the splicing of WT1 gene is present on Frasier syndrome patients with or without Wilms' tumorA S Barbosa, C G Hadjiathanasiou, C Theodoridis, et al.
The Journal of Pathology|March 19, 2008
FOXL2 and SOX9 as parameters of female and male gonadal differentiation in patients with various forms of disorders of sex development (DSD)R Hersmus, N Kalfa, B de Leeuw, et al.
American Journal of Human Genetics|August 27, 1998
Swyer syndrome and 46,XY partial gonadal dysgenesis associated with 9p deletions in the absence of monosomy-9p syndromeR A Veitia, M Nunes, L Quintana-Murci, et al.
Annals of Human Genetics|April 22, 2006
Population structure in the Mediterranean basin: a Y chromosome perspectiveC Capelli, N Redhead, V Romano, et al.
Pageof 25