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Charles Coutton

Showing results (11-20 of 133) with videos related to

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American Journal of Medical Genetics. Part A|March 21, 2014
Maternal complex chromosomal rearrangement leads to TCF12 microdeletion in a patient presenting with coronal craniosynostosis and intellectual disabilityPauline Le Tanno, Brice Poreau, Francoise Devillard, et al.
Asian Journal of Andrology|January 12, 2022
From azoospermia to macrozoospermia, a phenotypic continuum due to mutations in the <i>ZMYND15</i> geneZine-Eddine Kherraf, Caroline Cazin, Florence Lestrade, et al.
Basic and Clinical Andrology|March 18, 2015
Comparative testicular transcriptome of wild type and globozoospermic Dpy19l2 knock out miceThomas Karaouzène, Michèle El Atifi, Jean-Paul Issartel, et al.
European Journal of Pediatrics|July 3, 2014
Array-CGH in children with mild intellectual disability: a population-based studyCharles Coutton, Klaus Dieterich, Véronique Satre, et al.
Human Genetics|January 18, 2020
The genetic architecture of morphological abnormalities of the sperm tailAminata Touré, Guillaume Martinez, Zine-Eddine Kherraf, et al.
Psychiatric Genetics|December 18, 2023
Familial KCNQ2 mutation: a psychiatric perspectiveAnton Iftimovici, Angeline Charmet, Béatrice Desnous, et al.
Journal of Medical Primatology|June 12, 2020
Deslorelin acetate implant induces transient sterility and behavior changes in male olive baboon (Papio anubis): A case studyGuillaume Martinez, Romain Lacoste, Marie Dumasy, et al.
American Journal of Medical Genetics. Part A|April 10, 2014
7p22.3 microdeletion disrupting SNX8 in a patient presenting with intellectual disability but no tetralogy of FallotJohn Rendu, Véronique Satre, Hervé Testard, et al.
American Journal of Medical Genetics. Part A|November 23, 2024
An Extended Phenotype of PPP1R13L Cardiocutaneous SyndromeAlicia Coudert, Julien Thevenon, Quentin Testard, et al.
Clinical Genetics|December 20, 2022
Expanding the sperm phenotype caused by mutations in SPATA20: A novel splicing mutation in an infertile patient with partial globozoospermiaGuillaume Martinez, Catherine Metzler-Guillemain, Caroline Cazin, et al.
Pageof 14

Showing results (11-20 of 133) with videos related to

Sort By:
Pageof 14
American Journal of Medical Genetics. Part A|March 21, 2014
Maternal complex chromosomal rearrangement leads to TCF12 microdeletion in a patient presenting with coronal craniosynostosis and intellectual disabilityPauline Le Tanno, Brice Poreau, Francoise Devillard, et al.
Asian Journal of Andrology|January 12, 2022
From azoospermia to macrozoospermia, a phenotypic continuum due to mutations in the <i>ZMYND15</i> geneZine-Eddine Kherraf, Caroline Cazin, Florence Lestrade, et al.
Basic and Clinical Andrology|March 18, 2015
Comparative testicular transcriptome of wild type and globozoospermic Dpy19l2 knock out miceThomas Karaouzène, Michèle El Atifi, Jean-Paul Issartel, et al.
European Journal of Pediatrics|July 3, 2014
Array-CGH in children with mild intellectual disability: a population-based studyCharles Coutton, Klaus Dieterich, Véronique Satre, et al.
Human Genetics|January 18, 2020
The genetic architecture of morphological abnormalities of the sperm tailAminata Touré, Guillaume Martinez, Zine-Eddine Kherraf, et al.
Psychiatric Genetics|December 18, 2023
Familial KCNQ2 mutation: a psychiatric perspectiveAnton Iftimovici, Angeline Charmet, Béatrice Desnous, et al.
Journal of Medical Primatology|June 12, 2020
Deslorelin acetate implant induces transient sterility and behavior changes in male olive baboon (Papio anubis): A case studyGuillaume Martinez, Romain Lacoste, Marie Dumasy, et al.
American Journal of Medical Genetics. Part A|April 10, 2014
7p22.3 microdeletion disrupting SNX8 in a patient presenting with intellectual disability but no tetralogy of FallotJohn Rendu, Véronique Satre, Hervé Testard, et al.
American Journal of Medical Genetics. Part A|November 23, 2024
An Extended Phenotype of PPP1R13L Cardiocutaneous SyndromeAlicia Coudert, Julien Thevenon, Quentin Testard, et al.
Clinical Genetics|December 20, 2022
Expanding the sperm phenotype caused by mutations in SPATA20: A novel splicing mutation in an infertile patient with partial globozoospermiaGuillaume Martinez, Catherine Metzler-Guillemain, Caroline Cazin, et al.
Pageof 14