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Annales De Medecine Interne
|
January 1, 1982
[Double deficiency of sulfite and xanthine oxidase causing encephalopathy and due to a hereditary anomaly in the metabolism of molybdenum]
H Ogier, J M Saudubray, C Charpentier, et al.
Human Genetics
|
April 1, 1995
Exclusion of the cone-specific alpha-subunit of the transducin gene in Stargardt's disease
S Gerber, J M Rozet, D Bonneau, et al.
Annales De Biologie Clinique
|
January 1, 1988
[Genetic counseling in ornithine carbamoyltransferase deficiency]
A Pelet, E Toumas, D Rabier, et al.
Archives Francaises De Pediatrie
|
December 1, 1981
[Lysinuric protein intolerance: a severe hyperammonemia secondary to l-arginine deficiency (author's transl)]]
F X Coude, H Ogier, C Charpentier, et al.
Lancet (London, England)
|
August 4, 1990
Mapping of acute (type I) spinal muscular atrophy to chromosome 5q12-q14. The French Spinal Muscular Atrophy Investigators
J Melki, P Sheth, S Abdelhak, et al.
Human Genetics
|
January 1, 1980
Assignment of the genes for human lysosomal acid lipases A and B to chromosomes 10 and 16
V C Nguyen, D Weil, M C Hors-Cayla, et al.
Lancet (London, England)
|
September 3, 1988
Deletion of blood mitochondrial DNA in pancytopenia
A Rötig, M Colonna, S Blanche, et al.
Journal of Medical Genetics
|
March 1, 1994
Stargardt's disease is not allelic to the genes for neuronal ceroid lipofuscinoses
S Gerber, S Odent, A Postel-Vinay, et al.
Journal De Genetique Humaine
|
November 1, 1976
[The genetics of congenital glaucoma: a study of 231 cases]
M L Briard, J Feingold, J Kaplan, et al.
Human Genetics
|
January 1, 1981
Neonatal glutaric aciduria type II: an X-linked recessive inherited disorder
F X Coude, H Ogier, C Charpentier, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 61) with videos related to
Sort By:
Page
of 7
Annales De Medecine Interne
|
January 1, 1982
[Double deficiency of sulfite and xanthine oxidase causing encephalopathy and due to a hereditary anomaly in the metabolism of molybdenum]
H Ogier, J M Saudubray, C Charpentier, et al.
Human Genetics
|
April 1, 1995
Exclusion of the cone-specific alpha-subunit of the transducin gene in Stargardt's disease
S Gerber, J M Rozet, D Bonneau, et al.
Annales De Biologie Clinique
|
January 1, 1988
[Genetic counseling in ornithine carbamoyltransferase deficiency]
A Pelet, E Toumas, D Rabier, et al.
Archives Francaises De Pediatrie
|
December 1, 1981
[Lysinuric protein intolerance: a severe hyperammonemia secondary to l-arginine deficiency (author's transl)]]
F X Coude, H Ogier, C Charpentier, et al.
Lancet (London, England)
|
August 4, 1990
Mapping of acute (type I) spinal muscular atrophy to chromosome 5q12-q14. The French Spinal Muscular Atrophy Investigators
J Melki, P Sheth, S Abdelhak, et al.
Human Genetics
|
January 1, 1980
Assignment of the genes for human lysosomal acid lipases A and B to chromosomes 10 and 16
V C Nguyen, D Weil, M C Hors-Cayla, et al.
Lancet (London, England)
|
September 3, 1988
Deletion of blood mitochondrial DNA in pancytopenia
A Rötig, M Colonna, S Blanche, et al.
Journal of Medical Genetics
|
March 1, 1994
Stargardt's disease is not allelic to the genes for neuronal ceroid lipofuscinoses
S Gerber, S Odent, A Postel-Vinay, et al.
Journal De Genetique Humaine
|
November 1, 1976
[The genetics of congenital glaucoma: a study of 231 cases]
M L Briard, J Feingold, J Kaplan, et al.
Human Genetics
|
January 1, 1981
Neonatal glutaric aciduria type II: an X-linked recessive inherited disorder
F X Coude, H Ogier, C Charpentier, et al.
Page
of 7