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Gastroenterology
|
December 28, 1999
Vitamin D-receptor genotypes as independent genetic predictors of decreased bone mineral density in primary biliary cirrhosis
J E Springer, D E Cole, L A Rubin, et al.
Henry Ford Hospital Medical Journal
|
January 1, 1992
Screening for multiple endocrine neoplasia type 2A with DNA-polymorphism analysis
E M Lamothe, S A Narod, S Miller, et al.
Leukemia
|
June 1, 1994
Differentiation stages of childhood acute lymphoblastic leukemias with p53 mutations
C A Felix, R Wasserman, B J Lange, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
November 25, 2000
Alleles of the estrogen receptor alpha-gene and an estrogen receptor cotranscriptional activator gene, amplified in breast cancer-1 (AIB1), are associated with quantitative calcaneal ultrasound
M S Patel, D E Cole, J D Smith, et al.
American Journal of Human Genetics
|
January 1, 1997
mtDNA and Y chromosome-specific polymorphisms in modern Ojibwa: implications about the origin of their gene pool
R Scozzari, F Cruciani, P Santolamazza, et al.
American Journal of Human Genetics
|
September 1, 1996
Linkage disequilibrium analysis in young populations: pseudo-vitamin D-deficiency rickets and the founder effect in French Canadians
M Labuda, D Labuda, M Korab-Laskowska, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
March 1, 1990
Characterization of immunoglobulin and T-cell receptor gene patterns in B-cell precursor acute lymphoblastic leukemia of childhood
C A Felix, D G Poplack, G H Reaman, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 1, 1986
Secretory dysfunction in parathyroid cells from a neonate with severe primary hyperparathyroidism
S J Marx, R D Lasker, E M Brown, et al.
American Journal of Medical Genetics
|
June 28, 1996
Heteroallelic missense mutations of the galactosamine-6-sulfate sulfatase (GALNS) gene in a mild form of Morquio disease (MPS IVA)
D E Cole, S Fukuda, B A Gordon, et al.
Lancet (London, England)
|
February 19, 1999
A986S polymorphism of the calcium-sensing receptor and circulating calcium concentrations
D E Cole, V D Peltekova, L A Rubin, et al.
Page
of 17
Search research articles
Search
Showing results (141-150 of 162) with videos related to
Sort By:
Page
of 17
Gastroenterology
|
December 28, 1999
Vitamin D-receptor genotypes as independent genetic predictors of decreased bone mineral density in primary biliary cirrhosis
J E Springer, D E Cole, L A Rubin, et al.
Henry Ford Hospital Medical Journal
|
January 1, 1992
Screening for multiple endocrine neoplasia type 2A with DNA-polymorphism analysis
E M Lamothe, S A Narod, S Miller, et al.
Leukemia
|
June 1, 1994
Differentiation stages of childhood acute lymphoblastic leukemias with p53 mutations
C A Felix, R Wasserman, B J Lange, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
November 25, 2000
Alleles of the estrogen receptor alpha-gene and an estrogen receptor cotranscriptional activator gene, amplified in breast cancer-1 (AIB1), are associated with quantitative calcaneal ultrasound
M S Patel, D E Cole, J D Smith, et al.
American Journal of Human Genetics
|
January 1, 1997
mtDNA and Y chromosome-specific polymorphisms in modern Ojibwa: implications about the origin of their gene pool
R Scozzari, F Cruciani, P Santolamazza, et al.
American Journal of Human Genetics
|
September 1, 1996
Linkage disequilibrium analysis in young populations: pseudo-vitamin D-deficiency rickets and the founder effect in French Canadians
M Labuda, D Labuda, M Korab-Laskowska, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
March 1, 1990
Characterization of immunoglobulin and T-cell receptor gene patterns in B-cell precursor acute lymphoblastic leukemia of childhood
C A Felix, D G Poplack, G H Reaman, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 1, 1986
Secretory dysfunction in parathyroid cells from a neonate with severe primary hyperparathyroidism
S J Marx, R D Lasker, E M Brown, et al.
American Journal of Medical Genetics
|
June 28, 1996
Heteroallelic missense mutations of the galactosamine-6-sulfate sulfatase (GALNS) gene in a mild form of Morquio disease (MPS IVA)
D E Cole, S Fukuda, B A Gordon, et al.
Lancet (London, England)
|
February 19, 1999
A986S polymorphism of the calcium-sensing receptor and circulating calcium concentrations
D E Cole, V D Peltekova, L A Rubin, et al.
Page
of 17