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D E Cole

Showing results (141-150 of 162) with videos related to

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Gastroenterology|December 28, 1999
Vitamin D-receptor genotypes as independent genetic predictors of decreased bone mineral density in primary biliary cirrhosisJ 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 analysisE M Lamothe, S A Narod, S Miller, et al.
Leukemia|June 1, 1994
Differentiation stages of childhood acute lymphoblastic leukemias with p53 mutationsC 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 ultrasoundM 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 poolR 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 CanadiansM 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 childhoodC 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 hyperparathyroidismS 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 concentrationsD E Cole, V D Peltekova, L A Rubin, et al.
Pageof 17

Showing results (141-150 of 162) with videos related to

Sort By:
Pageof 17
Gastroenterology|December 28, 1999
Vitamin D-receptor genotypes as independent genetic predictors of decreased bone mineral density in primary biliary cirrhosisJ 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 analysisE M Lamothe, S A Narod, S Miller, et al.
Leukemia|June 1, 1994
Differentiation stages of childhood acute lymphoblastic leukemias with p53 mutationsC 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 ultrasoundM 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 poolR 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 CanadiansM 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 childhoodC 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 hyperparathyroidismS 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 concentrationsD E Cole, V D Peltekova, L A Rubin, et al.
Pageof 17