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Yves Morel

Showing results (11-20 of 92) with videos related to

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Fertility and Sterility|June 15, 2010
Transmissible microdeletion of the Y-chromosome encompassing two DAZ copies, four RBMY1 copies, and both PRY copiesIngrid Plotton, Claude Ducros, Michel Pugeat, et al.
The Journal of Clinical Endocrinology and Metabolism|June 8, 2006
Impaired sexual activity in male adults with partial androgen insensitivityClaire Bouvattier, Brigitte Mignot, Hervé Lefèvre, et al.
Hormone Research|February 24, 2006
Puberty in subjects with complete androgen insensitivity syndromeDimitrios T Papadimitriou, Agnès Linglart, Yves Morel, et al.
Annales D'Endocrinologie|July 25, 2016
Establishment of revised diagnostic cut-offs for adrenal laboratory investigation using the new Roche Diagnostics Elecsys<sup>®</sup> Cortisol II assayVéronique Raverot, Caroline Richet, Yves Morel, et al.
Annales D'Endocrinologie|January 24, 2015
A late 17α-hydroxylase deficiency diagnosis that leads to the discovery of a new CYP17 gene mutationAgathe Guenego, Yves Morel, Oana Ionesco, et al.
European Journal of Pediatrics|November 16, 2011
Congenital lipoid adrenal hyperplasia (a rare form of adrenal insufficiency and ambiguous genitalia) caused by a novel mutation of the steroidogenic acute regulatory protein geneOksana Lekarev, Delphine Mallet, Tony Yuen, et al.
Fertility and Sterility|May 16, 2002
Relation between the anatomical genital phenotype and cystic fibrosis transmembrane conductance regulator gene mutations in the absence of the vas deferensFrançois Robert, Faïza Bey-Omar, Jacques Rollet, et al.
Annales D'Endocrinologie|May 9, 2016
Evolution of steroids during pregnancy: Maternal, placental and fetal synthesisYves Morel, Florence Roucher, Ingrid Plotton, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|December 2, 2005
A novel 13-bp deletion in exon 1 of CYP21 gene causing severe congenital adrenal hyperplasiaMaher Kharrat, Véronique Tardy, Ridha M'rad, et al.
Clinical Chemistry and Laboratory Medicine|November 1, 2008
CYP21A2 gene mutation analysis in Moroccan patients with classic form of 21-hydroxylase deficiency: high regional prevalence of p.Q318X mutation and identification of a novel p.L353R mutationFatima Abid, Véronique Tardy, Ahmed Gaouzi, et al.
Pageof 10

Showing results (11-20 of 92) with videos related to

Sort By:
Pageof 10
Fertility and Sterility|June 15, 2010
Transmissible microdeletion of the Y-chromosome encompassing two DAZ copies, four RBMY1 copies, and both PRY copiesIngrid Plotton, Claude Ducros, Michel Pugeat, et al.
The Journal of Clinical Endocrinology and Metabolism|June 8, 2006
Impaired sexual activity in male adults with partial androgen insensitivityClaire Bouvattier, Brigitte Mignot, Hervé Lefèvre, et al.
Hormone Research|February 24, 2006
Puberty in subjects with complete androgen insensitivity syndromeDimitrios T Papadimitriou, Agnès Linglart, Yves Morel, et al.
Annales D'Endocrinologie|July 25, 2016
Establishment of revised diagnostic cut-offs for adrenal laboratory investigation using the new Roche Diagnostics Elecsys<sup>®</sup> Cortisol II assayVéronique Raverot, Caroline Richet, Yves Morel, et al.
Annales D'Endocrinologie|January 24, 2015
A late 17α-hydroxylase deficiency diagnosis that leads to the discovery of a new CYP17 gene mutationAgathe Guenego, Yves Morel, Oana Ionesco, et al.
European Journal of Pediatrics|November 16, 2011
Congenital lipoid adrenal hyperplasia (a rare form of adrenal insufficiency and ambiguous genitalia) caused by a novel mutation of the steroidogenic acute regulatory protein geneOksana Lekarev, Delphine Mallet, Tony Yuen, et al.
Fertility and Sterility|May 16, 2002
Relation between the anatomical genital phenotype and cystic fibrosis transmembrane conductance regulator gene mutations in the absence of the vas deferensFrançois Robert, Faïza Bey-Omar, Jacques Rollet, et al.
Annales D'Endocrinologie|May 9, 2016
Evolution of steroids during pregnancy: Maternal, placental and fetal synthesisYves Morel, Florence Roucher, Ingrid Plotton, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|December 2, 2005
A novel 13-bp deletion in exon 1 of CYP21 gene causing severe congenital adrenal hyperplasiaMaher Kharrat, Véronique Tardy, Ridha M'rad, et al.
Clinical Chemistry and Laboratory Medicine|November 1, 2008
CYP21A2 gene mutation analysis in Moroccan patients with classic form of 21-hydroxylase deficiency: high regional prevalence of p.Q318X mutation and identification of a novel p.L353R mutationFatima Abid, Véronique Tardy, Ahmed Gaouzi, et al.
Pageof 10