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Philippe Bouchard

Showing results (201-210 of 206) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|December 22, 2009
A comparative phenotypic study of kallmann syndrome patients carrying monoallelic and biallelic mutations in the prokineticin 2 or prokineticin receptor 2 genesJulie Sarfati, Anne Guiochon-Mantel, Philippe Rondard, et al.
The Journal of Clinical Endocrinology and Metabolism|December 15, 2010
Phenotypical, biological, and molecular heterogeneity of 5α-reductase deficiency: an extensive international experience of 55 patientsLaurent Maimoun, Pascal Philibert, Benoit Cammas, et al.
Human Mutation|July 22, 2008
Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndromeDiane Beysen, Sarah De Jaegere, David Amor, et al.
Human Molecular Genetics|February 5, 2013
Higher risk of death among MEN1 patients with mutations in the JunD interacting domain: a Groupe d'etude des Tumeurs Endocrines (GTE) cohort studyJulien Thevenon, Abderrahmane Bourredjem, Laurence Faivre, et al.
Journal of Clinical Periodontology|May 5, 2025
Consensus Report of the 20th European Workshop on Periodontology: Contemporary and Emerging Technologies in Periodontal DiagnosisDavid Herrera, Maurizio S Tonetti, Iain Chapple, et al.
Canadian Journal of Surgery. Journal Canadien De Chirurgie|November 28, 2024
2024 Canadian Surgery Forum: Sept. 25-28, 2024Christine Li, Michael Guo, Ahmer Karimuddin, et al.
Pageof 21

Showing results (201-210 of 206) with videos related to

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Pageof 21
You have reached the last page of results.This site can display upto 206 results.
The Journal of Clinical Endocrinology and Metabolism|December 22, 2009
A comparative phenotypic study of kallmann syndrome patients carrying monoallelic and biallelic mutations in the prokineticin 2 or prokineticin receptor 2 genesJulie Sarfati, Anne Guiochon-Mantel, Philippe Rondard, et al.
The Journal of Clinical Endocrinology and Metabolism|December 15, 2010
Phenotypical, biological, and molecular heterogeneity of 5α-reductase deficiency: an extensive international experience of 55 patientsLaurent Maimoun, Pascal Philibert, Benoit Cammas, et al.
Human Mutation|July 22, 2008
Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndromeDiane Beysen, Sarah De Jaegere, David Amor, et al.
Human Molecular Genetics|February 5, 2013
Higher risk of death among MEN1 patients with mutations in the JunD interacting domain: a Groupe d'etude des Tumeurs Endocrines (GTE) cohort studyJulien Thevenon, Abderrahmane Bourredjem, Laurence Faivre, et al.
Journal of Clinical Periodontology|May 5, 2025
Consensus Report of the 20th European Workshop on Periodontology: Contemporary and Emerging Technologies in Periodontal DiagnosisDavid Herrera, Maurizio S Tonetti, Iain Chapple, et al.
Canadian Journal of Surgery. Journal Canadien De Chirurgie|November 28, 2024
2024 Canadian Surgery Forum: Sept. 25-28, 2024Christine Li, Michael Guo, Ahmer Karimuddin, et al.
Pageof 21