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A Munnich

Showing results (61-70 of 573) with videos related to

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Human Molecular Genetics|September 15, 1998
The role of the SMN gene in proximal spinal muscular atrophyS Lefebvre, L Bürglen, J Frézal, et al.
Journal Francais D'Ophtalmologie|January 1, 1996
[Rapid demonstration of mutations previously identified in parents at risk of patients with autosomic dominant retinitis pigmentosa]E Souied, J M Rozet, S Gerber, et al.
Annales D'Endocrinologie|January 1, 1996
[Mutations of FGFR3 gene cause 3 types of nanisms with variably severity: achondroplasia, thanatophoric nanism and hypochondroplasia]F Rousseau, J Bonaventure, M Le Merrer, et al.
Progress in Clinical and Biological Research|January 1, 1982
New trends in the treatment of inborn errors of metabolism: an overviewJ Frézal, A Munnich, H Ogier, et al.
Journal of Medical Genetics|September 8, 2001
Mitochondrial DNA inheritance in patients with deleted mtDNAL Quintana-Murci, A Rötig, A Munnich, et al.
Human Molecular Genetics|June 1, 1994
DsaI polymorphism at the human cone transducin alpha-subunit (GNAT2) detected by PCRJ M Rozet, S Gerber, D Bonneau, et al.
The Journal of Biological Chemistry|December 15, 1987
Differential effects of glucose and fructose on liver L-type pyruvate kinase gene expression in vivoA Munnich, S Lyonnet, D Chauvet, et al.
Medical Hypotheses|June 22, 2000
Improvement of cystic fibrosis using antitumoral drugs: a hypothesisL Faivre, J P Bonnefont, S Lyonnet, et al.
Lancet (London, England)|June 27, 1998
Iron overload and mitochondrial diseasesP Rustin, J C von Kleist-Retzow, A Rötig, et al.
Human Genetics|October 1, 1990
Clinical and genetic heterogeneity in retinitis pigmentosaJ Kaplan, D Bonneau, J Frézal, et al.
Pageof 58

Showing results (61-70 of 573) with videos related to

Sort By:
Pageof 58
Human Molecular Genetics|September 15, 1998
The role of the SMN gene in proximal spinal muscular atrophyS Lefebvre, L Bürglen, J Frézal, et al.
Journal Francais D'Ophtalmologie|January 1, 1996
[Rapid demonstration of mutations previously identified in parents at risk of patients with autosomic dominant retinitis pigmentosa]E Souied, J M Rozet, S Gerber, et al.
Annales D'Endocrinologie|January 1, 1996
[Mutations of FGFR3 gene cause 3 types of nanisms with variably severity: achondroplasia, thanatophoric nanism and hypochondroplasia]F Rousseau, J Bonaventure, M Le Merrer, et al.
Progress in Clinical and Biological Research|January 1, 1982
New trends in the treatment of inborn errors of metabolism: an overviewJ Frézal, A Munnich, H Ogier, et al.
Journal of Medical Genetics|September 8, 2001
Mitochondrial DNA inheritance in patients with deleted mtDNAL Quintana-Murci, A Rötig, A Munnich, et al.
Human Molecular Genetics|June 1, 1994
DsaI polymorphism at the human cone transducin alpha-subunit (GNAT2) detected by PCRJ M Rozet, S Gerber, D Bonneau, et al.
The Journal of Biological Chemistry|December 15, 1987
Differential effects of glucose and fructose on liver L-type pyruvate kinase gene expression in vivoA Munnich, S Lyonnet, D Chauvet, et al.
Medical Hypotheses|June 22, 2000
Improvement of cystic fibrosis using antitumoral drugs: a hypothesisL Faivre, J P Bonnefont, S Lyonnet, et al.
Lancet (London, England)|June 27, 1998
Iron overload and mitochondrial diseasesP Rustin, J C von Kleist-Retzow, A Rötig, et al.
Human Genetics|October 1, 1990
Clinical and genetic heterogeneity in retinitis pigmentosaJ Kaplan, D Bonneau, J Frézal, et al.
Pageof 58