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Michael P Whyte

Showing results (121-130 of 165) with videos related to

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The Journal of Clinical Investigation|September 17, 2005
An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidismMichael R Bowl, M Andrew Nesbit, Brian Harding, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 28, 2020
ZNF687 Mutations in an Extended Cohort of Neoplastic Transformations in Paget's Disease of Bone: Implications for Clinical PathologyFederica Scotto di Carlo, Laura Pazzaglia, Steven Mumm, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 2, 2009
Chronic recurrent multifocal osteomyelitis mimicked in childhood hypophosphatasiaMichael P Whyte, Deborah Wenkert, William H McAlister, et al.
Lancet (London, England)|January 22, 2019
Skeletal fluorosis in a resettled refugee from Kakuma refugee campGabriel E Fabreau, Paul Bauman, Annalee L Coakley, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 23, 2018
Unique Variant of NOD2 Pediatric Granulomatous Arthritis With Severe 1,25-Dihydroxyvitamin D-Mediated Hypercalcemia and Generalized OsteosclerosisMichael P Whyte, Emilina Lim, William H McAlister, et al.
American Journal of Medical Genetics. Part A|October 14, 2005
Skeletal changes in epidermal nevus syndrome: does focal bone disease harbor clues concerning pathogenesis?Carrie L Heike, Michael L Cunningham, Robert D Steiner, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 13, 2014
Rapid skeletal turnover in a radiographic mimic of osteopetrosisMichael P Whyte, Katherine L Madson, Steven Mumm, et al.
Human Genetics|October 26, 2005
Mapping autosomal dominant progressive limb-girdle myopathy with bone fragility to chromosome 9p21-p22: a novel locus for a musculoskeletal syndromeGiles D J Watts, Sarju G Mehta, Chengfeng Zhao, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 14, 2012
Severe skeletal toxicity from protracted etidronate therapy for generalized arterial calcification of infancyJesse E Otero, Gary S Gottesman, William H McAlister, et al.
The New England Journal of Medicine|January 11, 2002
Paternally inherited inactivating mutations of the GNAS1 gene in progressive osseous heteroplasiaEileen M Shore, Jaimo Ahn, Suzanne Jan de Beur, et al.
Pageof 17

Showing results (121-130 of 165) with videos related to

Sort By:
Pageof 17
The Journal of Clinical Investigation|September 17, 2005
An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidismMichael R Bowl, M Andrew Nesbit, Brian Harding, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 28, 2020
ZNF687 Mutations in an Extended Cohort of Neoplastic Transformations in Paget's Disease of Bone: Implications for Clinical PathologyFederica Scotto di Carlo, Laura Pazzaglia, Steven Mumm, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 2, 2009
Chronic recurrent multifocal osteomyelitis mimicked in childhood hypophosphatasiaMichael P Whyte, Deborah Wenkert, William H McAlister, et al.
Lancet (London, England)|January 22, 2019
Skeletal fluorosis in a resettled refugee from Kakuma refugee campGabriel E Fabreau, Paul Bauman, Annalee L Coakley, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 23, 2018
Unique Variant of NOD2 Pediatric Granulomatous Arthritis With Severe 1,25-Dihydroxyvitamin D-Mediated Hypercalcemia and Generalized OsteosclerosisMichael P Whyte, Emilina Lim, William H McAlister, et al.
American Journal of Medical Genetics. Part A|October 14, 2005
Skeletal changes in epidermal nevus syndrome: does focal bone disease harbor clues concerning pathogenesis?Carrie L Heike, Michael L Cunningham, Robert D Steiner, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 13, 2014
Rapid skeletal turnover in a radiographic mimic of osteopetrosisMichael P Whyte, Katherine L Madson, Steven Mumm, et al.
Human Genetics|October 26, 2005
Mapping autosomal dominant progressive limb-girdle myopathy with bone fragility to chromosome 9p21-p22: a novel locus for a musculoskeletal syndromeGiles D J Watts, Sarju G Mehta, Chengfeng Zhao, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 14, 2012
Severe skeletal toxicity from protracted etidronate therapy for generalized arterial calcification of infancyJesse E Otero, Gary S Gottesman, William H McAlister, et al.
The New England Journal of Medicine|January 11, 2002
Paternally inherited inactivating mutations of the GNAS1 gene in progressive osseous heteroplasiaEileen M Shore, Jaimo Ahn, Suzanne Jan de Beur, et al.
Pageof 17