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L Villard

Showing results (51-60 of 99) with videos related to

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American Journal of Medical Genetics|July 9, 1999
Carpenter-Waziri syndrome results from a mutation in XNPF Abidi, C E Schwartz, N J Carpenter, et al.
American Journal of Medical Genetics. Part A|September 15, 2005
Delineation of the clinical phenotype associated with OPHN1 mutations based on the clinical and neuropsychological evaluation of three familiesB Chabrol, N Girard, K N'Guyen, et al.
Revue Neurologique|March 20, 2016
Severe neonatal seizures: From molecular diagnosis to precision therapy?M Milh, P Cacciagli, C Ravix, et al.
Neurology|November 9, 2000
Two affected boys in a Rett syndrome family: clinical and molecular findingsL Villard, A Kpebe, C Cardoso, et al.
Transactions of the Royal Society of Tropical Medicine and Hygiene|January 1, 1984
Seasonal variations in plasma retinol and carotenoid levels in rural Gambian womenC J Bates, L Villard, A M Prentice, et al.
American Journal of Human Genetics|March 1, 1996
Splicing mutation in the ATR-X gene can lead to a dysmorphic mental retardation phenotype without alpha-thalassemiaL Villard, A Toutain, A M Lossi, et al.
Bulletin De La Federation Des Societes De Gynecologie Et Dobstetrique De Langue Francaise|January 1, 1971
[Mulleroblastomas. Apropos of 2 cases]J Magré, P Leroux, M Lerat, et al.
International Journal for Vitamin and Nutrition Research. Internationale Zeitschrift Fur Vitamin- Und Ernahrungsforschung. Journal International De Vitaminologie Et De Nutrition|January 1, 1982
Physiological tests during an improvement in riboflavin status in lactating Gambian womenC J Bates, A M Prentice, A Prentice, et al.
Human Mutation|October 26, 1999
A polymorphic microsatellite XNP-GT in the XNP/ATRX gene's promotor allows familial indirect diagnosisN Lévy, R Bernard-Bronsard, A M Lossi, et al.
Laboratory Animal Science|March 25, 1999
Identification by 16S rDNA fragment amplification and determination of genetic diversity by random amplified polymorphic DNA analysis of Pasteurella pneumotropica isolated from laboratory rodentsA Kodjo, L Villard, F Veillet, et al.
Pageof 10

Showing results (51-60 of 99) with videos related to

Sort By:
Pageof 10
American Journal of Medical Genetics|July 9, 1999
Carpenter-Waziri syndrome results from a mutation in XNPF Abidi, C E Schwartz, N J Carpenter, et al.
American Journal of Medical Genetics. Part A|September 15, 2005
Delineation of the clinical phenotype associated with OPHN1 mutations based on the clinical and neuropsychological evaluation of three familiesB Chabrol, N Girard, K N'Guyen, et al.
Revue Neurologique|March 20, 2016
Severe neonatal seizures: From molecular diagnosis to precision therapy?M Milh, P Cacciagli, C Ravix, et al.
Neurology|November 9, 2000
Two affected boys in a Rett syndrome family: clinical and molecular findingsL Villard, A Kpebe, C Cardoso, et al.
Transactions of the Royal Society of Tropical Medicine and Hygiene|January 1, 1984
Seasonal variations in plasma retinol and carotenoid levels in rural Gambian womenC J Bates, L Villard, A M Prentice, et al.
American Journal of Human Genetics|March 1, 1996
Splicing mutation in the ATR-X gene can lead to a dysmorphic mental retardation phenotype without alpha-thalassemiaL Villard, A Toutain, A M Lossi, et al.
Bulletin De La Federation Des Societes De Gynecologie Et Dobstetrique De Langue Francaise|January 1, 1971
[Mulleroblastomas. Apropos of 2 cases]J Magré, P Leroux, M Lerat, et al.
International Journal for Vitamin and Nutrition Research. Internationale Zeitschrift Fur Vitamin- Und Ernahrungsforschung. Journal International De Vitaminologie Et De Nutrition|January 1, 1982
Physiological tests during an improvement in riboflavin status in lactating Gambian womenC J Bates, A M Prentice, A Prentice, et al.
Human Mutation|October 26, 1999
A polymorphic microsatellite XNP-GT in the XNP/ATRX gene's promotor allows familial indirect diagnosisN Lévy, R Bernard-Bronsard, A M Lossi, et al.
Laboratory Animal Science|March 25, 1999
Identification by 16S rDNA fragment amplification and determination of genetic diversity by random amplified polymorphic DNA analysis of Pasteurella pneumotropica isolated from laboratory rodentsA Kodjo, L Villard, F Veillet, et al.
Pageof 10