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P Malzac

Showing results (11-20 of 33) with videos related to

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Human Molecular Genetics|February 1, 1994
A novel splice site mutation in the first exon of the cystic fibrosis transmembrane regulator (CFTR) gene identified in a CBAVD patientJ F Culard, M Desgeorges, M C Romey, et al.
American Journal of Medical Genetics|July 24, 1998
Atypical molecular findings identify limits of technical screening tests for Prader-Willi and Angelman syndrome diagnosesP Malzac, A Moncla, K Pedeillier, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|May 1, 2010
Parental experience following perinatal death: exploring the issues to make progressM A Einaudi, P Le Coz, P Malzac, et al.
Human Reproduction (Oxford, England)|September 26, 2003
A balanced complex chromosomal rearrangement (BCCR) in a family with reproductive failureJ Lespinasse, M O North, C Paravy, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Clinical heterogeneity in 16 patients with inv dup 15 chromosome: cytogenetic and molecular studies, search for an imprinting effectC Mignon, P Malzac, A Moncla, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 1, 1994
[Angelman syndrome]A Moncla, M O Livet, P Malzac, et al.
American Journal of Medical Genetics|November 14, 2000
Genetic homogeneity of the urofacial (Ochoa) syndrome confirmed in a new French familyX Chauve, C Missirian, P Malzac, et al.
Gynecologie, Obstetrique & Fertilite|March 26, 2011
[Decision-making in termination of pregnancy: a French perspective]G Gorincour, S Tassy, A Payot, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Unexpected inheritance of the (CGG)n trinucleotide expansion in a fragile X syndrome familyP Malzac, V Biancalana, M A Voelckel, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Prader-Willi syndrome: diagnostic strategy with a cytogenetic and molecular approachP Malzac, A Moncla, M A Voelckel, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
Human Molecular Genetics|February 1, 1994
A novel splice site mutation in the first exon of the cystic fibrosis transmembrane regulator (CFTR) gene identified in a CBAVD patientJ F Culard, M Desgeorges, M C Romey, et al.
American Journal of Medical Genetics|July 24, 1998
Atypical molecular findings identify limits of technical screening tests for Prader-Willi and Angelman syndrome diagnosesP Malzac, A Moncla, K Pedeillier, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|May 1, 2010
Parental experience following perinatal death: exploring the issues to make progressM A Einaudi, P Le Coz, P Malzac, et al.
Human Reproduction (Oxford, England)|September 26, 2003
A balanced complex chromosomal rearrangement (BCCR) in a family with reproductive failureJ Lespinasse, M O North, C Paravy, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Clinical heterogeneity in 16 patients with inv dup 15 chromosome: cytogenetic and molecular studies, search for an imprinting effectC Mignon, P Malzac, A Moncla, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 1, 1994
[Angelman syndrome]A Moncla, M O Livet, P Malzac, et al.
American Journal of Medical Genetics|November 14, 2000
Genetic homogeneity of the urofacial (Ochoa) syndrome confirmed in a new French familyX Chauve, C Missirian, P Malzac, et al.
Gynecologie, Obstetrique & Fertilite|March 26, 2011
[Decision-making in termination of pregnancy: a French perspective]G Gorincour, S Tassy, A Payot, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Unexpected inheritance of the (CGG)n trinucleotide expansion in a fragile X syndrome familyP Malzac, V Biancalana, M A Voelckel, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Prader-Willi syndrome: diagnostic strategy with a cytogenetic and molecular approachP Malzac, A Moncla, M A Voelckel, et al.
Pageof 4