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S Barbaux

Showing results (21-30 of 36) with videos related to

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Human Genetics|October 1, 1995
Testicular development in an SRY-negative 46,XX individual harboring a distal Xp deletionA Tar, J Sólyom, B Györvári, et al.
Atherosclerosis|July 27, 2001
The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrationsD J Gaughan, L A Kluijtmans, S Barbaux, et al.
Annals of Human Genetics|December 4, 2003
SELPLG gene polymorphisms in relation to plasma SELPLG levels and coronary artery diseaseD A Tregouet, S Barbaux, O Poirier, et al.
Genomics|April 15, 1997
Gene sequence, localization, and evolutionary conservation of DAZLA, a candidate male sterility geneE Seboun, S Barbaux, T Bourgeron, et al.
Journal of Developmental Origins of Health and Disease|July 24, 2014
Placental expression of the obesity-associated gene FTO is reduced by fetal growth restriction but not by macrosomia in rats and humansS Mayeur, O Cisse, A Gabory, et al.
Human Genetics|May 1, 1997
Mutations and sequence variants in the testis-determining region of the Y chromosome in individuals with a 46,XY female phenotypeR Veitia, A Ion, S Barbaux, et al.
Placenta|December 17, 2009
Cullins in human intra-uterine growth restriction: expressional and epigenetic alterationsG Gascoin-Lachambre, C Buffat, R Rebourcet, et al.
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 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.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
Human Genetics|October 1, 1995
Testicular development in an SRY-negative 46,XX individual harboring a distal Xp deletionA Tar, J Sólyom, B Györvári, et al.
Atherosclerosis|July 27, 2001
The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrationsD J Gaughan, L A Kluijtmans, S Barbaux, et al.
Annals of Human Genetics|December 4, 2003
SELPLG gene polymorphisms in relation to plasma SELPLG levels and coronary artery diseaseD A Tregouet, S Barbaux, O Poirier, et al.
Genomics|April 15, 1997
Gene sequence, localization, and evolutionary conservation of DAZLA, a candidate male sterility geneE Seboun, S Barbaux, T Bourgeron, et al.
Journal of Developmental Origins of Health and Disease|July 24, 2014
Placental expression of the obesity-associated gene FTO is reduced by fetal growth restriction but not by macrosomia in rats and humansS Mayeur, O Cisse, A Gabory, et al.
Human Genetics|May 1, 1997
Mutations and sequence variants in the testis-determining region of the Y chromosome in individuals with a 46,XY female phenotypeR Veitia, A Ion, S Barbaux, et al.
Placenta|December 17, 2009
Cullins in human intra-uterine growth restriction: expressional and epigenetic alterationsG Gascoin-Lachambre, C Buffat, R Rebourcet, et al.
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 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.
Pageof 4