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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 hybridization
V 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 region
P 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 children
M 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 descent
M C Romey, M Desgeorges, P Malzac, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 33) with videos related to
Sort By:
Page
of 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 hybridization
V 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 region
P 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 children
M 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 descent
M C Romey, M Desgeorges, P Malzac, et al.
Page
of 4