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P Edery

Showing results (11-20 of 54) with videos related to

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Clinical Genetics|November 4, 2004
Autosomal dominant B-cell immunodeficiency, distal limb anomalies and urogenital malformations (BILU syndrome) - report of a second familyM Tischkowitz, F Goodman, M Koliou, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 5, 2001
[Diagnostic trap and difficulties of genetic counseling in a family with neuromuscular disease carriers]G Lesca, E Ollagnon-Roman, J Lachanat, et al.
Journal of Medical Genetics|April 1, 1995
Exclusion of RET and Pax 3 loci in Waardenburg-Hirschsprung diseaseT Attié, M Till, A Pelet, et al.
American Journal of Medical Genetics|August 15, 1994
Apparent genetic homogeneity of the Treacher Collins-Franceschetti syndromeP Edery, Y Manach, M Le Merrer, et al.
L'Encephale|December 20, 2014
[Neurocognitive and psychiatric management of the 22q11.2 deletion syndrome]C Demily, M Rossi, M Schneider, et al.
Human Molecular Genetics|December 1, 1995
Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung diseaseT Attié, M Till, A Pelet, et al.
Studies in Health Technology and Informatics|June 15, 2010
Recent advances in the study of candidate genes for adolescent idiopathic scoliosisK Fendri, S Patten, C Zaouter, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1996
[Genetics of Hirschsprung disease]T Attié, R Salomon, J Amiel, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 29, 2001
[Genetic deafness:the primary cause of sensorineural hearing loss in children]G Lina-Granade, L Morlé, N Alloisio, et al.
American Journal of Medical Genetics|October 20, 2000
Ectodermal abnormalities associated with methimazole intrauterine exposureT Martin-Denavit, P Edery, H Plauchu, et al.
Pageof 6

Showing results (11-20 of 54) with videos related to

Sort By:
Pageof 6
Clinical Genetics|November 4, 2004
Autosomal dominant B-cell immunodeficiency, distal limb anomalies and urogenital malformations (BILU syndrome) - report of a second familyM Tischkowitz, F Goodman, M Koliou, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 5, 2001
[Diagnostic trap and difficulties of genetic counseling in a family with neuromuscular disease carriers]G Lesca, E Ollagnon-Roman, J Lachanat, et al.
Journal of Medical Genetics|April 1, 1995
Exclusion of RET and Pax 3 loci in Waardenburg-Hirschsprung diseaseT Attié, M Till, A Pelet, et al.
American Journal of Medical Genetics|August 15, 1994
Apparent genetic homogeneity of the Treacher Collins-Franceschetti syndromeP Edery, Y Manach, M Le Merrer, et al.
L'Encephale|December 20, 2014
[Neurocognitive and psychiatric management of the 22q11.2 deletion syndrome]C Demily, M Rossi, M Schneider, et al.
Human Molecular Genetics|December 1, 1995
Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung diseaseT Attié, M Till, A Pelet, et al.
Studies in Health Technology and Informatics|June 15, 2010
Recent advances in the study of candidate genes for adolescent idiopathic scoliosisK Fendri, S Patten, C Zaouter, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1996
[Genetics of Hirschsprung disease]T Attié, R Salomon, J Amiel, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 29, 2001
[Genetic deafness:the primary cause of sensorineural hearing loss in children]G Lina-Granade, L Morlé, N Alloisio, et al.
American Journal of Medical Genetics|October 20, 2000
Ectodermal abnormalities associated with methimazole intrauterine exposureT Martin-Denavit, P Edery, H Plauchu, et al.
Pageof 6