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Stanislas Lyonnet

Showing results (61-70 of 260) with videos related to

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Human Molecular Genetics|August 12, 2008
Human neural crest cells display molecular and phenotypic hallmarks of stem cellsSophie Thomas, Marie Thomas, Patrick Wincker, et al.
Cancer Letters|June 14, 2005
Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastomaFranck Bourdeaut, Delphine Trochet, Isabelle Janoueix-Lerosey, et al.
American Journal of Medical Genetics. Part A|November 5, 2003
Werner mesomelic dysplasia with Hirschsprung diseaseAlice Goldenberg, Mathieu Milh, Pascal de Lagausie, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 13, 2005
Clinical and molecular overlap in overgrowth syndromesGeneviève Baujat, Marlène Rio, Sylvie Rossignol, et al.
American Journal of Medical Genetics. Part A|October 27, 2019
Expanding the phenotype in Adams-Oliver syndrome correlating with the genotypeBenjamin Dudoignon, Celine Huber, Caroline Michot, et al.
American Journal of Human Genetics|April 17, 2007
Mutations in TCF4, encoding a class I basic helix-loop-helix transcription factor, are responsible for Pitt-Hopkins syndrome, a severe epileptic encephalopathy associated with autonomic dysfunctionJeanne Amiel, Marlene Rio, Loic de Pontual, et al.
American Journal of Medical Genetics. Part A|April 8, 2015
RPL10 mutation segregating in a family with X-linked syndromic Intellectual DisabilityJulien Thevenon, Caroline Michot, Christine Bole, et al.
Frontiers in Pharmacology|April 11, 2022
Patient-Patient Similarity-Based Screening of a Clinical Data Warehouse to Support Ciliopathy DiagnosisXiaoyi Chen, Carole Faviez, Marc Vincent, et al.
American Journal of Medical Genetics. Part A|November 22, 2017
MED13L loss-of-function variants in two patients with syndromic Pierre Robin sequenceChristopher T Gordon, Maya Chopra, Myriam Oufadem, et al.
Journal of Medical Genetics|August 24, 2019
<i>De novo</i> SCAMP5 mutation causes a neurodevelopmental disorder with autistic features and seizuresLaurence Hubert, Magda Cannata Serio, Laure Villoing-Gaudé, et al.
Pageof 26

Showing results (61-70 of 260) with videos related to

Sort By:
Pageof 26
Human Molecular Genetics|August 12, 2008
Human neural crest cells display molecular and phenotypic hallmarks of stem cellsSophie Thomas, Marie Thomas, Patrick Wincker, et al.
Cancer Letters|June 14, 2005
Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastomaFranck Bourdeaut, Delphine Trochet, Isabelle Janoueix-Lerosey, et al.
American Journal of Medical Genetics. Part A|November 5, 2003
Werner mesomelic dysplasia with Hirschsprung diseaseAlice Goldenberg, Mathieu Milh, Pascal de Lagausie, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 13, 2005
Clinical and molecular overlap in overgrowth syndromesGeneviève Baujat, Marlène Rio, Sylvie Rossignol, et al.
American Journal of Medical Genetics. Part A|October 27, 2019
Expanding the phenotype in Adams-Oliver syndrome correlating with the genotypeBenjamin Dudoignon, Celine Huber, Caroline Michot, et al.
American Journal of Human Genetics|April 17, 2007
Mutations in TCF4, encoding a class I basic helix-loop-helix transcription factor, are responsible for Pitt-Hopkins syndrome, a severe epileptic encephalopathy associated with autonomic dysfunctionJeanne Amiel, Marlene Rio, Loic de Pontual, et al.
American Journal of Medical Genetics. Part A|April 8, 2015
RPL10 mutation segregating in a family with X-linked syndromic Intellectual DisabilityJulien Thevenon, Caroline Michot, Christine Bole, et al.
Frontiers in Pharmacology|April 11, 2022
Patient-Patient Similarity-Based Screening of a Clinical Data Warehouse to Support Ciliopathy DiagnosisXiaoyi Chen, Carole Faviez, Marc Vincent, et al.
American Journal of Medical Genetics. Part A|November 22, 2017
MED13L loss-of-function variants in two patients with syndromic Pierre Robin sequenceChristopher T Gordon, Maya Chopra, Myriam Oufadem, et al.
Journal of Medical Genetics|August 24, 2019
<i>De novo</i> SCAMP5 mutation causes a neurodevelopmental disorder with autistic features and seizuresLaurence Hubert, Magda Cannata Serio, Laure Villoing-Gaudé, et al.
Pageof 26