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American Journal of Medical Genetics
|
August 1, 1984
A private view of heterozygosity: eight-year follow-up study on carriers of the Tay-Sachs gene detected by high school screening in Montreal
S Zeesman, C L Clow, L Cartier, et al.
Nucleic Acids Research
|
January 25, 1991
A rapid procedure for extracting genomic DNA from leukocytes
S W John, G Weitzner, R Rozen, et al.
The Journal of Clinical Investigation
|
November 1, 1971
Transport and metabolism of sarcosine in hypersarcosinemic and normal phenotypes
F H Glorieux, C R Scriver, E Delvin, et al.
Pediatrics
|
January 1, 1972
A filter paper sampling method for the uric acid:creatinine ratio in urine. Normal values in the the newborn
R McInnes, P Lamm, C L Clow, et al.
Canadian Medical Association Journal
|
May 5, 1973
The frequency of genetic disease and congenital malformation among patients in a pediatric hospital
C R Scriver, J L Neal, R Saginur, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 1, 1987
Lysinuric protein intolerance mutation is expressed in the plasma membrane of cultured skin fibroblasts
D W Smith, C R Scriver, H S Tenenhouse, et al.
American Journal of Human Genetics
|
May 1, 1989
Prolidase deficiency: biochemical classification of alleles
A P Boright, C R Scriver, G A Lancaster, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 15, 1977
Evaluation of metabolic pathway activity in cultured skin fibroblasts and blood leukocytes
R Rozen, S Buhl, F Mohyuddin, et al.
Annual Review of Genetics
|
January 1, 1994
The hyperphenylalaninemias of man and mouse
C R Scriver, R C Eisensmith, S L Woo, et al.
The New England Journal of Medicine
|
October 8, 1970
Cystinuria: increased prevalence in patients with mental disease
C R Scriver, D T Whelan, C L Clow, et al.
Page
of 32
Search research articles
Search
Showing results (211-220 of 317) with videos related to
Sort By:
Page
of 32
American Journal of Medical Genetics
|
August 1, 1984
A private view of heterozygosity: eight-year follow-up study on carriers of the Tay-Sachs gene detected by high school screening in Montreal
S Zeesman, C L Clow, L Cartier, et al.
Nucleic Acids Research
|
January 25, 1991
A rapid procedure for extracting genomic DNA from leukocytes
S W John, G Weitzner, R Rozen, et al.
The Journal of Clinical Investigation
|
November 1, 1971
Transport and metabolism of sarcosine in hypersarcosinemic and normal phenotypes
F H Glorieux, C R Scriver, E Delvin, et al.
Pediatrics
|
January 1, 1972
A filter paper sampling method for the uric acid:creatinine ratio in urine. Normal values in the the newborn
R McInnes, P Lamm, C L Clow, et al.
Canadian Medical Association Journal
|
May 5, 1973
The frequency of genetic disease and congenital malformation among patients in a pediatric hospital
C R Scriver, J L Neal, R Saginur, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 1, 1987
Lysinuric protein intolerance mutation is expressed in the plasma membrane of cultured skin fibroblasts
D W Smith, C R Scriver, H S Tenenhouse, et al.
American Journal of Human Genetics
|
May 1, 1989
Prolidase deficiency: biochemical classification of alleles
A P Boright, C R Scriver, G A Lancaster, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 15, 1977
Evaluation of metabolic pathway activity in cultured skin fibroblasts and blood leukocytes
R Rozen, S Buhl, F Mohyuddin, et al.
Annual Review of Genetics
|
January 1, 1994
The hyperphenylalaninemias of man and mouse
C R Scriver, R C Eisensmith, S L Woo, et al.
The New England Journal of Medicine
|
October 8, 1970
Cystinuria: increased prevalence in patients with mental disease
C R Scriver, D T Whelan, C L Clow, et al.
Page
of 32