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American Journal of Human Genetics
|
February 1, 1988
The ornithine aminotransferase (OAT) locus: analysis of RFLPs in gyrate atrophy
V Ramesh, L A Benoit, P Crawford, et al.
Prenatal Diagnosis
|
May 1, 1996
Use of amniotic fluid amino acids in prenatal testing for argininosuccinic aciduria and citrullinaemia
R Mandell, S Packman, R Laframboise, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 1, 1988
Molecular basis of ornithine aminotransferase deficiency in B-6-responsive and -nonresponsive forms of gyrate atrophy
V Ramesh, A I McClatchey, N Ramesh, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
January 1, 1992
Mapping of ornithine aminotransferase gene sequences to mouse chromosomes 7, X, and 3
V Ramesh, S V Cheng, C A Kozak, et al.
American Journal of Human Genetics
|
May 1, 1983
The prognosis of hyperlysinemia: an interim report
J Dancis, J Hutzler, M G Ampola, et al.
American Journal of Human Genetics
|
November 1, 1990
Splicing defect at the ornithine aminotransferase (OAT) locus in gyrate atrophy
A I McClatchey, D L Kaufman, E L Berson, et al.
Prenatal Diagnosis
|
July 1, 1986
Prenatal diagnosis of non-ketotic hyperglycinemia
D A Applegarth, H L Levy, V E Shih, et al.
Archives of Neurology
|
September 1, 1992
An antispasticity effect of threonine in multiple sclerosis
S L Hauser, T H Doolittle, M Lopez-Bresnahan, et al.
Transplantation
|
October 31, 2001
Vascular endothelial function in cyclosporine and tacrolimus treated renal transplant recipients
C A Ovuworie, E R Fox, C M Chow, et al.
The New England Journal of Medicine
|
April 8, 1971
Galactosemia screening of newborns in Massachusetts
V E Shih, H I Levy, V Karolkewicz, et al.
Page
of 12
Search research articles
Search
Showing results (91-100 of 112) with videos related to
Sort By:
Page
of 12
American Journal of Human Genetics
|
February 1, 1988
The ornithine aminotransferase (OAT) locus: analysis of RFLPs in gyrate atrophy
V Ramesh, L A Benoit, P Crawford, et al.
Prenatal Diagnosis
|
May 1, 1996
Use of amniotic fluid amino acids in prenatal testing for argininosuccinic aciduria and citrullinaemia
R Mandell, S Packman, R Laframboise, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 1, 1988
Molecular basis of ornithine aminotransferase deficiency in B-6-responsive and -nonresponsive forms of gyrate atrophy
V Ramesh, A I McClatchey, N Ramesh, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
January 1, 1992
Mapping of ornithine aminotransferase gene sequences to mouse chromosomes 7, X, and 3
V Ramesh, S V Cheng, C A Kozak, et al.
American Journal of Human Genetics
|
May 1, 1983
The prognosis of hyperlysinemia: an interim report
J Dancis, J Hutzler, M G Ampola, et al.
American Journal of Human Genetics
|
November 1, 1990
Splicing defect at the ornithine aminotransferase (OAT) locus in gyrate atrophy
A I McClatchey, D L Kaufman, E L Berson, et al.
Prenatal Diagnosis
|
July 1, 1986
Prenatal diagnosis of non-ketotic hyperglycinemia
D A Applegarth, H L Levy, V E Shih, et al.
Archives of Neurology
|
September 1, 1992
An antispasticity effect of threonine in multiple sclerosis
S L Hauser, T H Doolittle, M Lopez-Bresnahan, et al.
Transplantation
|
October 31, 2001
Vascular endothelial function in cyclosporine and tacrolimus treated renal transplant recipients
C A Ovuworie, E R Fox, C M Chow, et al.
The New England Journal of Medicine
|
April 8, 1971
Galactosemia screening of newborns in Massachusetts
V E Shih, H I Levy, V Karolkewicz, et al.
Page
of 12