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P Malzac

Showing results (1-10 of 26) with videos related to

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Ethique & Sante|August 25, 2020
[What support for vulnerable people during confinement?]P Malzac, M Mathieu, M A Einaudi
Human Genetics|March 1, 1996
Chromosomal localization of the human and mouse histidine decarboxylase genes by in situ hybridization. Exclusion of the HDC gene from the Prader-Willi syndrome regionP Malzac, M G Mattei, J Thibault, et al.
Annales De L'Anesthesiologie Francaise|January 1, 1976
[Hemodynamic effects of high-dosage corticoids. Their justification in the treatment of shock]J du Cailar, J Kienlen, P Malzac, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 1, 1997
[Smith-Magenis syndrome]D Lacombe, A Moncla, P Malzac, et al.
Hormone Research|January 9, 2001
Auxological and endocrine evolution of 28 children with Prader-Willi syndrome: effect of GH therapy in 14 childrenM Tauber, C Barbeau, B Jouret, 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.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Ethique & Sante|August 25, 2020
[What support for vulnerable people during confinement?]P Malzac, M Mathieu, M A Einaudi
Human Genetics|March 1, 1996
Chromosomal localization of the human and mouse histidine decarboxylase genes by in situ hybridization. Exclusion of the HDC gene from the Prader-Willi syndrome regionP Malzac, M G Mattei, J Thibault, et al.
Annales De L'Anesthesiologie Francaise|January 1, 1976
[Hemodynamic effects of high-dosage corticoids. Their justification in the treatment of shock]J du Cailar, J Kienlen, P Malzac, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 1, 1997
[Smith-Magenis syndrome]D Lacombe, A Moncla, P Malzac, et al.
Hormone Research|January 9, 2001
Auxological and endocrine evolution of 28 children with Prader-Willi syndrome: effect of GH therapy in 14 childrenM Tauber, C Barbeau, B Jouret, 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.
Pageof 3