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A Munnich

Showing results (41-50 of 573) with videos related to

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Journal of Medical Genetics|August 1, 1995
Filippi syndrome: a new case with skeletal abnormalitiesD Héron, T Billette de Villemeur, A Munnich, et al.
The Journal of Biological Chemistry|September 15, 1993
Fate and expression of the deleted mitochondrial DNA differ between human heteroplasmic skin fibroblast and Epstein-Barr virus-transformed lymphocyte culturesT Bourgeron, D Chretien, A Rötig, et al.
Presse Medicale (Paris, France : 1983)|November 2, 1996
[Advances in genetics: what benefits children?]S Lyonnet, J P Bonnefont, M L Briard, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 1, 1996
[Rise of genetics: what are the benefits for children?]S Lyonnet, J P Bonnefont, M L Briard, et al.
The Journal of Clinical Investigation|June 1, 1988
In vivo regulation of glycolytic and gluconeogenic enzyme gene expression in newborn rat liverS Lyonnet, C Coupé, J Girard, et al.
Bone|January 31, 2004
Overexpression of FGFR3, Stat1, Stat5 and p21Cip1 correlates with phenotypic severity and defective chondrocyte differentiation in FGFR3-related chondrodysplasiasL Legeai-Mallet, C Benoist-Lasselin, A Munnich, et al.
Human Molecular Genetics|December 1, 1992
A new 15 bp deletion in exon 11 of the phenylalanine hydroxylase gene in phenylketonuriaJ Jaruzelska, D Melle, R Matuszak, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 6, 1998
[Congenital malformations in pediatric tumors]J Amiel, D Lacombe, T Attié, et al.
Human Molecular Genetics|April 1, 1994
Novel frame shift deletions of the phenylalanine hydroxylase gene in phenylketonuriaP Bénit, F Rey, D Melle, et al.
Journal of Child Neurology|January 1, 1994
Leigh syndrome: pyruvate dehydrogenase defect. A case with peripheral neuropathyB Chabrol, J Mancini, C Benelli, et al.
Pageof 58

Showing results (41-50 of 573) with videos related to

Sort By:
Pageof 58
Journal of Medical Genetics|August 1, 1995
Filippi syndrome: a new case with skeletal abnormalitiesD Héron, T Billette de Villemeur, A Munnich, et al.
The Journal of Biological Chemistry|September 15, 1993
Fate and expression of the deleted mitochondrial DNA differ between human heteroplasmic skin fibroblast and Epstein-Barr virus-transformed lymphocyte culturesT Bourgeron, D Chretien, A Rötig, et al.
Presse Medicale (Paris, France : 1983)|November 2, 1996
[Advances in genetics: what benefits children?]S Lyonnet, J P Bonnefont, M L Briard, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 1, 1996
[Rise of genetics: what are the benefits for children?]S Lyonnet, J P Bonnefont, M L Briard, et al.
The Journal of Clinical Investigation|June 1, 1988
In vivo regulation of glycolytic and gluconeogenic enzyme gene expression in newborn rat liverS Lyonnet, C Coupé, J Girard, et al.
Bone|January 31, 2004
Overexpression of FGFR3, Stat1, Stat5 and p21Cip1 correlates with phenotypic severity and defective chondrocyte differentiation in FGFR3-related chondrodysplasiasL Legeai-Mallet, C Benoist-Lasselin, A Munnich, et al.
Human Molecular Genetics|December 1, 1992
A new 15 bp deletion in exon 11 of the phenylalanine hydroxylase gene in phenylketonuriaJ Jaruzelska, D Melle, R Matuszak, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 6, 1998
[Congenital malformations in pediatric tumors]J Amiel, D Lacombe, T Attié, et al.
Human Molecular Genetics|April 1, 1994
Novel frame shift deletions of the phenylalanine hydroxylase gene in phenylketonuriaP Bénit, F Rey, D Melle, et al.
Journal of Child Neurology|January 1, 1994
Leigh syndrome: pyruvate dehydrogenase defect. A case with peripheral neuropathyB Chabrol, J Mancini, C Benelli, et al.
Pageof 58