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F Jaubert

Showing results (121-130 of 143) with videos related to

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Lancet (London, England)|January 22, 1994
SRY-negative XX fetus with complete male phenotypeE Vilain, B Le Fiblec, N Morichon-Delvallez, et al.
Human Pathology|November 9, 2000
Anti-Müllerian hormone is a specific marker of sertoli- and granulosa-cell origin in gonadal tumorsR Rey, J C Sabourin, M Venara, et al.
Human Mutation|May 2, 2008
Spectrum of HLXB9 gene mutations in Currarino syndrome and genotype-phenotype correlationC Crétolle, A Pelet, D Sanlaville, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 31, 2002
Persistence of Müllerian remnants in complete androgen insensitivity syndromeD Damiani, M A Mascolli, M J Almeida, et al.
Journal of Medical Genetics|December 10, 2002
Evolution and expression of FOXL2J Cocquet, E Pailhoux, F Jaubert, et al.
Journal of Medical Genetics|January 31, 2006
Mutations of the RET gene in isolated and syndromic Hirschsprung's disease in human disclose major and modifier alleles at a single locusL de Pontual, A Pelet, D Trochet, 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.
Molecular Genetics and Metabolism|October 20, 2007
Development of liver disease despite mannose treatment in two patients with CDG-IbK Mention, F Lacaille, V Valayannopoulos, et al.
Neurogastroenterology and Motility|October 1, 2010
Normal oxidative phosphorylation in intestinal smooth muscle of childhood chronic intestinal pseudo-obstructionL Galmiche, F Jaubert, F Sauvat, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 4, 2005
[Congenital hyperinsulinism in newborn and infant]I Giurgea, M-J Ribeiro, N Boddaert, et al.
Pageof 15

Showing results (121-130 of 143) with videos related to

Sort By:
Pageof 15
Lancet (London, England)|January 22, 1994
SRY-negative XX fetus with complete male phenotypeE Vilain, B Le Fiblec, N Morichon-Delvallez, et al.
Human Pathology|November 9, 2000
Anti-Müllerian hormone is a specific marker of sertoli- and granulosa-cell origin in gonadal tumorsR Rey, J C Sabourin, M Venara, et al.
Human Mutation|May 2, 2008
Spectrum of HLXB9 gene mutations in Currarino syndrome and genotype-phenotype correlationC Crétolle, A Pelet, D Sanlaville, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 31, 2002
Persistence of Müllerian remnants in complete androgen insensitivity syndromeD Damiani, M A Mascolli, M J Almeida, et al.
Journal of Medical Genetics|December 10, 2002
Evolution and expression of FOXL2J Cocquet, E Pailhoux, F Jaubert, et al.
Journal of Medical Genetics|January 31, 2006
Mutations of the RET gene in isolated and syndromic Hirschsprung's disease in human disclose major and modifier alleles at a single locusL de Pontual, A Pelet, D Trochet, 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.
Molecular Genetics and Metabolism|October 20, 2007
Development of liver disease despite mannose treatment in two patients with CDG-IbK Mention, F Lacaille, V Valayannopoulos, et al.
Neurogastroenterology and Motility|October 1, 2010
Normal oxidative phosphorylation in intestinal smooth muscle of childhood chronic intestinal pseudo-obstructionL Galmiche, F Jaubert, F Sauvat, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 4, 2005
[Congenital hyperinsulinism in newborn and infant]I Giurgea, M-J Ribeiro, N Boddaert, et al.
Pageof 15