S Chantot-Bastaraud - JoVE Visualize

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Molecular Human Reproduction|May 12, 2007

Mutations in the protamine 1 gene associated with male infertilityC Ravel, S Chantot-Bastaraud, B El Houate, et al.

The Journal of Clinical Endocrinology and Metabolism|March 23, 2016

Deletion of CPEB1 Gene: A Rare but Recurrent Cause of Premature Ovarian InsufficiencyC Hyon, L Mansour-Hendili, S Chantot-Bastaraud, et al.

Annales De Genetique|July 18, 2002

French multi-centric study of 2000 amniotic fluid interphase FISH analyses from high-risk pregnancies and review of the literatureI Luquet, F Mugneret, P D Athis, et al.

Clinical Genetics|October 21, 2016

Xq28 duplication including MECP2 in six unreported affected females: what can we learn for diagnosis and genetic counselling?S El Chehadeh, R Touraine, F Prieur, et al.

Clinical Genetics|November 20, 2015

Genetic counselling difficulties and ethical implications of incidental findings from array-CGH: a 7-year national surveyM Lefebvre, D Sanlaville, N Marle, et al.

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Showing results (11-20 of 15) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 15 results.

Molecular Human Reproduction|May 12, 2007

Mutations in the protamine 1 gene associated with male infertilityC Ravel, S Chantot-Bastaraud, B El Houate, et al.

The Journal of Clinical Endocrinology and Metabolism|March 23, 2016

Deletion of CPEB1 Gene: A Rare but Recurrent Cause of Premature Ovarian InsufficiencyC Hyon, L Mansour-Hendili, S Chantot-Bastaraud, et al.

Annales De Genetique|July 18, 2002

French multi-centric study of 2000 amniotic fluid interphase FISH analyses from high-risk pregnancies and review of the literatureI Luquet, F Mugneret, P D Athis, et al.

Clinical Genetics|October 21, 2016

Xq28 duplication including MECP2 in six unreported affected females: what can we learn for diagnosis and genetic counselling?S El Chehadeh, R Touraine, F Prieur, et al.

Clinical Genetics|November 20, 2015

Genetic counselling difficulties and ethical implications of incidental findings from array-CGH: a 7-year national surveyM Lefebvre, D Sanlaville, N Marle, et al.

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