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S Lyonnet

Showing results (181-190 of 223) with videos related to

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The Journal of Pediatrics|July 11, 2001
Inversion of the circadian rhythm of melatonin in the Smith-Magenis syndromeH De Leersnyder, M C De Blois, B Claustrat, et al.
The Journal of Clinical Endocrinology and Metabolism|November 10, 2001
Spectrum of mutations of the AAAS gene in Allgrove syndrome: lack of mutations in six kindreds with isolated resistance to corticotropinF Sandrini, C Farmakidis, L S Kirschner, et al.
Clinical Genetics|April 10, 2002
A CGH study of 27 patients with CHARGE associationD Sanlaville, S P Romana, J M Lapierre, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|April 22, 2005
Idiopathic achalasia is not allelic to alacrima achalasia adrenal insufficiency syndrome at the ALADIN locusG Di Nardo, A Tullio-Pelet, V Annese, et al.
European Journal of Human Genetics : EJHG|August 22, 2000
Linkage disequilibrium in inbred North African families allows fine genetic and physical mapping of triple A syndromeS Hadj-Rabia, R Salomon, A Pelet, et al.
Journal of Medical Genetics|January 16, 1998
Features of DiGeorge syndrome and CHARGE association in five patientsP de Lonlay-Debeney, V Cormier-Daire, J Amiel, et al.
Journal of Medical Genetics|February 24, 2001
The mutation spectrum in Holt-Oram syndromeS J Cross, Y H Ching, Q Y Li, et al.
Clinical Genetics|July 31, 2007
Familial CHARGE syndrome because of CHD7 mutation: clinical intra- and interfamilial variabilityA Delahaye, Y Sznajer, S Lyonnet, et al.
Clinical Genetics|December 1, 1996
Increased paternal age in CHARGE associationA L Tellier, S Lyonnet, V Cormier-Daire, et al.
Journal of Medical Genetics|May 4, 2004
Embryonic expression of the human MID1 gene and its mutations in Opitz syndromeL Pinson, J Augé, S Audollent, et al.
Pageof 23

Showing results (181-190 of 223) with videos related to

Sort By:
Pageof 23
The Journal of Pediatrics|July 11, 2001
Inversion of the circadian rhythm of melatonin in the Smith-Magenis syndromeH De Leersnyder, M C De Blois, B Claustrat, et al.
The Journal of Clinical Endocrinology and Metabolism|November 10, 2001
Spectrum of mutations of the AAAS gene in Allgrove syndrome: lack of mutations in six kindreds with isolated resistance to corticotropinF Sandrini, C Farmakidis, L S Kirschner, et al.
Clinical Genetics|April 10, 2002
A CGH study of 27 patients with CHARGE associationD Sanlaville, S P Romana, J M Lapierre, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|April 22, 2005
Idiopathic achalasia is not allelic to alacrima achalasia adrenal insufficiency syndrome at the ALADIN locusG Di Nardo, A Tullio-Pelet, V Annese, et al.
European Journal of Human Genetics : EJHG|August 22, 2000
Linkage disequilibrium in inbred North African families allows fine genetic and physical mapping of triple A syndromeS Hadj-Rabia, R Salomon, A Pelet, et al.
Journal of Medical Genetics|January 16, 1998
Features of DiGeorge syndrome and CHARGE association in five patientsP de Lonlay-Debeney, V Cormier-Daire, J Amiel, et al.
Journal of Medical Genetics|February 24, 2001
The mutation spectrum in Holt-Oram syndromeS J Cross, Y H Ching, Q Y Li, et al.
Clinical Genetics|July 31, 2007
Familial CHARGE syndrome because of CHD7 mutation: clinical intra- and interfamilial variabilityA Delahaye, Y Sznajer, S Lyonnet, et al.
Clinical Genetics|December 1, 1996
Increased paternal age in CHARGE associationA L Tellier, S Lyonnet, V Cormier-Daire, et al.
Journal of Medical Genetics|May 4, 2004
Embryonic expression of the human MID1 gene and its mutations in Opitz syndromeL Pinson, J Augé, S Audollent, et al.
Pageof 23