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Patrick Calvas

Showing results (21-30 of 97) with videos related to

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Journal International De Bioethique Et D'Ethique Des Sciences|September 8, 2023
Myriam Guedj, Marion Rosier, Patrick Calvas, et al.
Investigative Ophthalmology & Visual Science|February 19, 2010
Identification of the IRXB gene cluster as candidate genes in severe dysgenesis of the ocular anterior segmentMyriam Chaabouni, Heather Etchevers, Marie Christine De Blois, et al.
The Journal of Investigative Dermatology|November 4, 2006
DNA-based prenatal diagnosis of harlequin ichthyosis and characterization of ABCA12 mutation consequencesMasashi Akiyama, Matthias Titeux, Kaori Sakai, et al.
Investigative Ophthalmology & Visual Science|June 17, 2011
Comparative transcriptome and network biology analyses demonstrate antiproliferative and hyperapoptotic phenotypes in human keratoconus corneasMatthias Macé, Stéphane D Galiacy, Angélique Erraud, et al.
European Journal of Medical Genetics|August 2, 2022
EPHA2 biallelic disruption causes syndromic complex microphthalmia with iris hypoplasiaCécile Courdier, Anna Gemahling, Damien Guindolet, et al.
European Journal of Medical Genetics|May 5, 2011
A 17q12 chromosomal duplication associated with renal disease and esophageal atresiaStanislas Faguer, Nicolas Chassaing, Flavio Bandin, et al.
Human Mutation|August 13, 2011
Digenic inheritance of mutations in FOXC1 and PITX2 : correlating transcription factor function and Axenfeld-Rieger disease severityDaniel Kelberman, Lily Islam, Susan E Holder, et al.
American Journal of Medical Genetics. Part A|April 23, 2016
Confirmation of TENM3 involvement in autosomal recessive colobomatous microphthalmiaNicolas Chassaing, Nicola Ragge, Julie Plaisancié, et al.
American Journal of Medical Genetics. Part A|May 7, 2024
ITPR1: The missing gene in miosis-ataxia syndrome?Bertrand Chesneau, Patrick Calvas, Myriam Cassagne, et al.
European Journal of Medical Genetics|November 27, 2013
Distal 10q monosomy: new evidence for a neurobehavioral condition?Julie Plaisancié, Laurence Bouneau, Claude Cances, et al.
Pageof 10

Showing results (21-30 of 97) with videos related to

Sort By:
Pageof 10
Journal International De Bioethique Et D'Ethique Des Sciences|September 8, 2023
Myriam Guedj, Marion Rosier, Patrick Calvas, et al.
Investigative Ophthalmology & Visual Science|February 19, 2010
Identification of the IRXB gene cluster as candidate genes in severe dysgenesis of the ocular anterior segmentMyriam Chaabouni, Heather Etchevers, Marie Christine De Blois, et al.
The Journal of Investigative Dermatology|November 4, 2006
DNA-based prenatal diagnosis of harlequin ichthyosis and characterization of ABCA12 mutation consequencesMasashi Akiyama, Matthias Titeux, Kaori Sakai, et al.
Investigative Ophthalmology & Visual Science|June 17, 2011
Comparative transcriptome and network biology analyses demonstrate antiproliferative and hyperapoptotic phenotypes in human keratoconus corneasMatthias Macé, Stéphane D Galiacy, Angélique Erraud, et al.
European Journal of Medical Genetics|August 2, 2022
EPHA2 biallelic disruption causes syndromic complex microphthalmia with iris hypoplasiaCécile Courdier, Anna Gemahling, Damien Guindolet, et al.
European Journal of Medical Genetics|May 5, 2011
A 17q12 chromosomal duplication associated with renal disease and esophageal atresiaStanislas Faguer, Nicolas Chassaing, Flavio Bandin, et al.
Human Mutation|August 13, 2011
Digenic inheritance of mutations in FOXC1 and PITX2 : correlating transcription factor function and Axenfeld-Rieger disease severityDaniel Kelberman, Lily Islam, Susan E Holder, et al.
American Journal of Medical Genetics. Part A|April 23, 2016
Confirmation of TENM3 involvement in autosomal recessive colobomatous microphthalmiaNicolas Chassaing, Nicola Ragge, Julie Plaisancié, et al.
American Journal of Medical Genetics. Part A|May 7, 2024
ITPR1: The missing gene in miosis-ataxia syndrome?Bertrand Chesneau, Patrick Calvas, Myriam Cassagne, et al.
European Journal of Medical Genetics|November 27, 2013
Distal 10q monosomy: new evidence for a neurobehavioral condition?Julie Plaisancié, Laurence Bouneau, Claude Cances, et al.
Pageof 10