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The Journal of Pediatrics
|
June 1, 1991
Primary oxaluria type 2 (L-glyceric aciduria): a rare cause of nephrolithiasis in children
L E Seargeant, G W deGroot, L A Dilling, et al.
The Journal of Pediatrics
|
August 1, 1971
Neonatal hypoglycemia: a discussion
A Beard, M Cornblath, J Gentz, et al.
Pediatrics
|
August 1, 1989
Newborn screening for galactosemia: a new method used in Manitoba
C R Greenberg, L A Dilling, R Thompson, et al.
Journal of Clinical Pathology
|
May 1, 1981
Routine bone marrow examination in the management of acute lymphoblastic leukaemia of childhood
C Haworth, A D Heppleston, P H Morris Jones, et al.
Clinical Genetics
|
March 1, 1997
Two novel mutations in a Canadian family with aspartylglucosaminuria and early outcome post bone marrow transplantation
A Laitinen, M Hietala, J C Haworth, et al.
Nature Cell Biology
|
December 17, 2009
Defects in DNA ligase I trigger PCNA ubiquitylation at Lys 107
Sapna Das-Bradoo, Hai Dang Nguyen, Jamie L Wood, et al.
Cancer Detection and Prevention
|
January 1, 1992
Sister chromatid exchange (SCE) frequency in lymphocytes of patients with colorectal carcinoma treated with razoxane
C M Price, D Hagger, M Evans, et al.
Journal of Virological Methods
|
November 7, 2000
Design and validation of immunological tests for the detection of Porcine endogenous retrovirus in biological materials
D N Galbraith, H T Kelly, A Dyke, et al.
American Journal of Human Genetics
|
February 1, 1990
Infantile hypophosphatasia: localization within chromosome region 1p36.1-34 and prenatal diagnosis using linked DNA markers
C R Greenberg, J A Evans, S McKendry-Smith, et al.
The New England Journal of Medicine
|
March 15, 1984
Homocystinuria and megaloblastic anemia responsive to vitamin B12 therapy. An inborn error of metabolism due to a defect in cobalamin metabolism
S Schuh, D S Rosenblatt, B A Cooper, et al.
Page
of 15
Search research articles
Search
Showing results (111-120 of 143) with videos related to
Sort By:
Page
of 15
The Journal of Pediatrics
|
June 1, 1991
Primary oxaluria type 2 (L-glyceric aciduria): a rare cause of nephrolithiasis in children
L E Seargeant, G W deGroot, L A Dilling, et al.
The Journal of Pediatrics
|
August 1, 1971
Neonatal hypoglycemia: a discussion
A Beard, M Cornblath, J Gentz, et al.
Pediatrics
|
August 1, 1989
Newborn screening for galactosemia: a new method used in Manitoba
C R Greenberg, L A Dilling, R Thompson, et al.
Journal of Clinical Pathology
|
May 1, 1981
Routine bone marrow examination in the management of acute lymphoblastic leukaemia of childhood
C Haworth, A D Heppleston, P H Morris Jones, et al.
Clinical Genetics
|
March 1, 1997
Two novel mutations in a Canadian family with aspartylglucosaminuria and early outcome post bone marrow transplantation
A Laitinen, M Hietala, J C Haworth, et al.
Nature Cell Biology
|
December 17, 2009
Defects in DNA ligase I trigger PCNA ubiquitylation at Lys 107
Sapna Das-Bradoo, Hai Dang Nguyen, Jamie L Wood, et al.
Cancer Detection and Prevention
|
January 1, 1992
Sister chromatid exchange (SCE) frequency in lymphocytes of patients with colorectal carcinoma treated with razoxane
C M Price, D Hagger, M Evans, et al.
Journal of Virological Methods
|
November 7, 2000
Design and validation of immunological tests for the detection of Porcine endogenous retrovirus in biological materials
D N Galbraith, H T Kelly, A Dyke, et al.
American Journal of Human Genetics
|
February 1, 1990
Infantile hypophosphatasia: localization within chromosome region 1p36.1-34 and prenatal diagnosis using linked DNA markers
C R Greenberg, J A Evans, S McKendry-Smith, et al.
The New England Journal of Medicine
|
March 15, 1984
Homocystinuria and megaloblastic anemia responsive to vitamin B12 therapy. An inborn error of metabolism due to a defect in cobalamin metabolism
S Schuh, D S Rosenblatt, B A Cooper, et al.
Page
of 15