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C Moutou

Showing results (1-10 of 39) with videos related to

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Prenatal Diagnosis|February 8, 2000
Improvement of preimplantation genetic diagnosis (PGD) for the cystic fibrosis mutation delta F508 by fluorescent polymerase chain reactionC Moutou, S Viville
Annales De Biologie Clinique|December 16, 2003
[Preimplantation genetic diagnosis of monogenic diseases]C Moutou, S Viville
Journal of Medical Genetics|April 1, 1992
Beckwith-Wiedemann syndrome: a demonstration of the mechanisms responsible for the excess of transmitting femalesC Moutou, C Junien, I Henry, et al.
Molecular Human Reproduction|November 23, 2006
Strategies and outcomes of PGD of familial adenomatous polyposisC Moutou, N Gardes, J-C Nicod, et al.
Human Molecular Genetics|July 1, 1997
Transition from premutation to full mutation in fragile X syndrome is likely to be prezygoticC Moutou, M C Vincent, V Biancalana, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 1, 1996
[Mental retardation in fragile X syndrome]J L Mandel, V Biancalana, M Cossée, et al.
Gynecologie, Obstetrique & Fertilite|December 6, 2001
[Twin birth after preimplantation diagnosis for cystic fibrosis]C Moutou, J Ohl, C Wittemer, et al.
Human Mutation|September 30, 1999
Identification of novel mutations in the MTM1 gene causing severe and mild forms of X-linked myotubular myopathyA Buj-Bello, V Biancalana, C Moutou, et al.
Genetic Epidemiology|January 1, 1995
ARCAD: a method for estimating age-dependent disease risk associated with mutation carrier status from family dataC Le Bihan, C Moutou, L Brugières, et al.
Human Reproduction (Oxford, England)|November 9, 2017
ESHRE PGD Consortium data collection XIV-XV: cycles from January 2011 to December 2012 with pregnancy follow-up to October 2013M De Rycke, V Goossens, G Kokkali, et al.
Pageof 4

Showing results (1-10 of 39) with videos related to

Sort By:
Pageof 4
Prenatal Diagnosis|February 8, 2000
Improvement of preimplantation genetic diagnosis (PGD) for the cystic fibrosis mutation delta F508 by fluorescent polymerase chain reactionC Moutou, S Viville
Annales De Biologie Clinique|December 16, 2003
[Preimplantation genetic diagnosis of monogenic diseases]C Moutou, S Viville
Journal of Medical Genetics|April 1, 1992
Beckwith-Wiedemann syndrome: a demonstration of the mechanisms responsible for the excess of transmitting femalesC Moutou, C Junien, I Henry, et al.
Molecular Human Reproduction|November 23, 2006
Strategies and outcomes of PGD of familial adenomatous polyposisC Moutou, N Gardes, J-C Nicod, et al.
Human Molecular Genetics|July 1, 1997
Transition from premutation to full mutation in fragile X syndrome is likely to be prezygoticC Moutou, M C Vincent, V Biancalana, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 1, 1996
[Mental retardation in fragile X syndrome]J L Mandel, V Biancalana, M Cossée, et al.
Gynecologie, Obstetrique & Fertilite|December 6, 2001
[Twin birth after preimplantation diagnosis for cystic fibrosis]C Moutou, J Ohl, C Wittemer, et al.
Human Mutation|September 30, 1999
Identification of novel mutations in the MTM1 gene causing severe and mild forms of X-linked myotubular myopathyA Buj-Bello, V Biancalana, C Moutou, et al.
Genetic Epidemiology|January 1, 1995
ARCAD: a method for estimating age-dependent disease risk associated with mutation carrier status from family dataC Le Bihan, C Moutou, L Brugières, et al.
Human Reproduction (Oxford, England)|November 9, 2017
ESHRE PGD Consortium data collection XIV-XV: cycles from January 2011 to December 2012 with pregnancy follow-up to October 2013M De Rycke, V Goossens, G Kokkali, et al.
Pageof 4