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Canadian Medical Association Journal
|
August 18, 1973
Variant maple syrup urine disease in mother and daughter
L A Zaleski, J Dancis, R P Cox, et al.
Experimental Cell Research
|
October 1, 1974
Incorporation of hypoxanthine by PHA-stimulated HPRT-deficient lymphocytes
R P Cox, M R Krauss, M E Balis, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1973
Unstable HPRTase in subjects with abnormal urinary oxypurine excretion
M E Balis, L C Yip, T F Yu, et al.
Pediatric Research
|
August 1, 1992
Transfer and metabolism of retinol by the perfused human placenta
J Dancis, M Levitz, J Katz, et al.
The Journal of Clinical Investigation
|
June 1, 1976
Hypoxanthine phosphoribosyltransferase activity in intact fibroblasts from patients with X-linked hyperuricemia
M J Holland, A M DiLorenzo, J Dancis, et al.
American Journal of Human Genetics
|
March 1, 1976
The occurrence of new mutants in the X-linked recessive Lesch-Nyhan disease
U Francke, J Felsenstein, S M Gartler, et al.
Pediatric Research
|
July 1, 1988
Zellweger syndrome amniocytes: morphological appearance and a simple sedimentation method for prenatal diagnosis
P B Lazarow, G M Small, M Santos, 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.
Annals of Internal Medicine
|
February 1, 1972
Rarity of X-linked partial hypoxanthine-guanine phosphoribosyltransferase deficiency in a large gouty population
T F Yü, M E Balis, T A Krenitsky, et al.
Pediatric Research
|
December 1, 1985
Zellweger syndrome: biochemical and morphological studies on two patients treated with clofibrate
P B Lazarow, V Black, H Shio, et al.
Page
of 12
Search research articles
Search
Showing results (111-120 of 120) with videos related to
Sort By:
Page
of 12
You have reached the last page of results.
This site can display upto 120 results.
Canadian Medical Association Journal
|
August 18, 1973
Variant maple syrup urine disease in mother and daughter
L A Zaleski, J Dancis, R P Cox, et al.
Experimental Cell Research
|
October 1, 1974
Incorporation of hypoxanthine by PHA-stimulated HPRT-deficient lymphocytes
R P Cox, M R Krauss, M E Balis, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1973
Unstable HPRTase in subjects with abnormal urinary oxypurine excretion
M E Balis, L C Yip, T F Yu, et al.
Pediatric Research
|
August 1, 1992
Transfer and metabolism of retinol by the perfused human placenta
J Dancis, M Levitz, J Katz, et al.
The Journal of Clinical Investigation
|
June 1, 1976
Hypoxanthine phosphoribosyltransferase activity in intact fibroblasts from patients with X-linked hyperuricemia
M J Holland, A M DiLorenzo, J Dancis, et al.
American Journal of Human Genetics
|
March 1, 1976
The occurrence of new mutants in the X-linked recessive Lesch-Nyhan disease
U Francke, J Felsenstein, S M Gartler, et al.
Pediatric Research
|
July 1, 1988
Zellweger syndrome amniocytes: morphological appearance and a simple sedimentation method for prenatal diagnosis
P B Lazarow, G M Small, M Santos, 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.
Annals of Internal Medicine
|
February 1, 1972
Rarity of X-linked partial hypoxanthine-guanine phosphoribosyltransferase deficiency in a large gouty population
T F Yü, M E Balis, T A Krenitsky, et al.
Pediatric Research
|
December 1, 1985
Zellweger syndrome: biochemical and morphological studies on two patients treated with clofibrate
P B Lazarow, V Black, H Shio, et al.
Page
of 12