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P Malzac

Showing results (1-10 of 33) with videos related to

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La Revue Du Praticien|December 16, 2000
[Prenatal diagnosis of genetic diseases. Indications, methods, legal and ethical aspects]P Malzac, J F Mattei
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 23, 2005
[Adoption: ethical bases of an awaited amendment]P Le Coz, P Malzac
Ethique & Sante|August 25, 2020
[What support for vulnerable people during confinement?]P Malzac, M Mathieu, M A Einaudi
Genomics|October 1, 1993
Localization of a novel ryanodine receptor gene (RYR3) to human chromosome 15q14-q15 by in situ hybridizationV Sorrentino, G Giannini, P Malzac, et al.
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.
Maroc Medical|June 1, 1970
[Hyperbaric oxygenation and carbon monoxide poisoning. Apropos of 100 cases]J Du Cailar, F Lefebvre, B Roquefeuil, 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.
Human Molecular Genetics|April 1, 1994
Homozygosity for a novel missense mutation (I175V) in exon 5 of the CFTR gene in a family of Armenian descentM C Romey, M Desgeorges, P Malzac, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
La Revue Du Praticien|December 16, 2000
[Prenatal diagnosis of genetic diseases. Indications, methods, legal and ethical aspects]P Malzac, J F Mattei
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 23, 2005
[Adoption: ethical bases of an awaited amendment]P Le Coz, P Malzac
Ethique & Sante|August 25, 2020
[What support for vulnerable people during confinement?]P Malzac, M Mathieu, M A Einaudi
Genomics|October 1, 1993
Localization of a novel ryanodine receptor gene (RYR3) to human chromosome 15q14-q15 by in situ hybridizationV Sorrentino, G Giannini, P Malzac, et al.
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.
Maroc Medical|June 1, 1970
[Hyperbaric oxygenation and carbon monoxide poisoning. Apropos of 100 cases]J Du Cailar, F Lefebvre, B Roquefeuil, 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.
Human Molecular Genetics|April 1, 1994
Homozygosity for a novel missense mutation (I175V) in exon 5 of the CFTR gene in a family of Armenian descentM C Romey, M Desgeorges, P Malzac, et al.
Pageof 4