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Clinical Genetics
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July 1, 1997
Incomplete penetrance and expressivity skewing in hereditary multiple exostoses
L Legeai-Mallet, A Munnich, P Maroteaux, et al.
Molecular and Cellular Biochemistry
|
October 6, 1997
Nicotinamide adenine dinucleotides permeate through mitochondrial membranes in human Epstein-Barr virus-transformed lymphocytes
P Rustin, D Chretien, B Parfait, et al.
Biochemical and Biophysical Research Communications
|
November 30, 1990
The measurement of the rotenone-sensitive NADH cytochrome c reductase activity in mitochondria isolated from minute amount of human skeletal muscle
D Chretien, T Bourgeron, A Rötig, et al.
Biochemical and Biophysical Research Communications
|
July 15, 1992
Isolation and characterization of mitochondria from human B lymphoblastoid cell lines
T Bourgeron, D Chretien, A Rötig, et al.
Human Mutation
|
January 1, 1994
Five novel missense mutations of the phenylalanine hydroxylase gene in phenylketonuria
P Bénit, F Rey, D Melle, et al.
Clinical Genetics
|
August 25, 2004
New insights in congenital bowing of the femora
V Cormier-Daire, D Geneviève, A Munnich, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
January 1, 1996
[Genetic diseases in mapping gene databases, genome interactive databases (GID)]
A Munnich, M Le Merrer, M L Chauvet, et al.
American Journal of Medical Genetics
|
September 1, 1992
Parental origin of the X chromosomes in Rett syndrome
L Benedetti, A Munnich, J Melki, et al.
Molecular Genetics and Metabolism
|
August 13, 1999
Human genes involved in chromatin remodeling in transcription initiation, and associated diseases: An overview using the GENATLAS database
M Roux-Rouquie, M L Chauvet, A Munnich, et al.
Molecular Genetics and Metabolism
|
April 18, 2000
Screening human EST database for identification of candidate genes in respiratory chain deficiency
A Rötig, I Valnot, C Mugnier, et al.
Page
of 58
Search research articles
Search
Showing results (51-60 of 573) with videos related to
Sort By:
Page
of 58
Clinical Genetics
|
July 1, 1997
Incomplete penetrance and expressivity skewing in hereditary multiple exostoses
L Legeai-Mallet, A Munnich, P Maroteaux, et al.
Molecular and Cellular Biochemistry
|
October 6, 1997
Nicotinamide adenine dinucleotides permeate through mitochondrial membranes in human Epstein-Barr virus-transformed lymphocytes
P Rustin, D Chretien, B Parfait, et al.
Biochemical and Biophysical Research Communications
|
November 30, 1990
The measurement of the rotenone-sensitive NADH cytochrome c reductase activity in mitochondria isolated from minute amount of human skeletal muscle
D Chretien, T Bourgeron, A Rötig, et al.
Biochemical and Biophysical Research Communications
|
July 15, 1992
Isolation and characterization of mitochondria from human B lymphoblastoid cell lines
T Bourgeron, D Chretien, A Rötig, et al.
Human Mutation
|
January 1, 1994
Five novel missense mutations of the phenylalanine hydroxylase gene in phenylketonuria
P Bénit, F Rey, D Melle, et al.
Clinical Genetics
|
August 25, 2004
New insights in congenital bowing of the femora
V Cormier-Daire, D Geneviève, A Munnich, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
January 1, 1996
[Genetic diseases in mapping gene databases, genome interactive databases (GID)]
A Munnich, M Le Merrer, M L Chauvet, et al.
American Journal of Medical Genetics
|
September 1, 1992
Parental origin of the X chromosomes in Rett syndrome
L Benedetti, A Munnich, J Melki, et al.
Molecular Genetics and Metabolism
|
August 13, 1999
Human genes involved in chromatin remodeling in transcription initiation, and associated diseases: An overview using the GENATLAS database
M Roux-Rouquie, M L Chauvet, A Munnich, et al.
Molecular Genetics and Metabolism
|
April 18, 2000
Screening human EST database for identification of candidate genes in respiratory chain deficiency
A Rötig, I Valnot, C Mugnier, et al.
Page
of 58