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P Edery

Showing results (31-40 of 54) with videos related to

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Journal of Medical Genetics|August 1, 1994
Long segment and short segment familial Hirschsprung's disease: variable clinical expression at the RET locusP Edery, A Pelet, L M Mulligan, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 3, 2015
[Smith-Magenis syndrome is an association of behavioral and sleep/wake circadian rhythm disorders]A Poisson, A Nicolas, D Sanlaville, et al.
Human Molecular Genetics|August 1, 1995
Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung diseaseT Attié, A Pelet, P Edery, et al.
Gastroenterologie Clinique Et Biologique|January 1, 1997
[Mutations of the endothelin-3 gene in isolated and syndromic forms of Hirschsprung disease]C Bidaud, R Salomon, P Edery, et al.
American Journal of Human Genetics|October 18, 2000
A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15L Morlé, M Bozon, J C Zech, et al.
Lancet (London, England)|September 6, 2000
Quinone-responsive multiple respiratory-chain dysfunction due to widespread coenzyme Q10 deficiencyA Rötig, E L Appelkvist, V Geromel, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|April 1, 1994
[Mutations of RET proto-oncogene in Hirschsprung disease]S Lyonnet, P Edery, L M Mulligan, et al.
Nature|January 27, 1994
Mutations of the RET proto-oncogene in Hirschsprung's diseaseP Edery, S Lyonnet, L M Mulligan, et al.
Prenatal Diagnosis|November 25, 1998
Prenatal diagnosis of an 8p23.1 deletion in a fetus with a diaphragmatic hernia and review of the literatureL Faivre, N Morichon-Delvallez, G Viot, et al.
Neuropediatrics|May 1, 1999
Respiratory chain deficiency presenting as recurrent myoglobinuria in childhoodP de Lonlay-Debeney, P Edery, V Cormier-Daire, et al.
Pageof 6

Showing results (31-40 of 54) with videos related to

Sort By:
Pageof 6
Journal of Medical Genetics|August 1, 1994
Long segment and short segment familial Hirschsprung's disease: variable clinical expression at the RET locusP Edery, A Pelet, L M Mulligan, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 3, 2015
[Smith-Magenis syndrome is an association of behavioral and sleep/wake circadian rhythm disorders]A Poisson, A Nicolas, D Sanlaville, et al.
Human Molecular Genetics|August 1, 1995
Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung diseaseT Attié, A Pelet, P Edery, et al.
Gastroenterologie Clinique Et Biologique|January 1, 1997
[Mutations of the endothelin-3 gene in isolated and syndromic forms of Hirschsprung disease]C Bidaud, R Salomon, P Edery, et al.
American Journal of Human Genetics|October 18, 2000
A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15L Morlé, M Bozon, J C Zech, et al.
Lancet (London, England)|September 6, 2000
Quinone-responsive multiple respiratory-chain dysfunction due to widespread coenzyme Q10 deficiencyA Rötig, E L Appelkvist, V Geromel, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|April 1, 1994
[Mutations of RET proto-oncogene in Hirschsprung disease]S Lyonnet, P Edery, L M Mulligan, et al.
Nature|January 27, 1994
Mutations of the RET proto-oncogene in Hirschsprung's diseaseP Edery, S Lyonnet, L M Mulligan, et al.
Prenatal Diagnosis|November 25, 1998
Prenatal diagnosis of an 8p23.1 deletion in a fetus with a diaphragmatic hernia and review of the literatureL Faivre, N Morichon-Delvallez, G Viot, et al.
Neuropediatrics|May 1, 1999
Respiratory chain deficiency presenting as recurrent myoglobinuria in childhoodP de Lonlay-Debeney, P Edery, V Cormier-Daire, et al.
Pageof 6