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P Whyte

Showing results (391-400 of 454) with videos related to

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Bone|May 16, 2019
New explanation for autosomal dominant high bone mass: Mutation of low-density lipoprotein receptor-related protein 6Michael P Whyte, William H McAlister, Fan Zhang, et al.
European Journal of Human Genetics : EJHG|October 8, 2009
Comparison of human chromosome 19q13 and syntenic region on mouse chromosome 7 reveals absence, in man, of 11.6 Mb containing four mouse calcium-sensing receptor-related sequences: relevance to familial benign hypocalciuric hypercalcaemia type 3Fadil M Hannan, M Andrew Nesbit, Jeremy J O Turner, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 31, 2012
Enzyme replacement prevents enamel defects in hypophosphatasia miceManisha C Yadav, Rodrigo Cardoso de Oliveira, Brian L Foster, et al.
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.
Epidemiology and Infection|April 21, 2006
Antibiotic resistance of retail food and human Campylobacter isolates on the island of Ireland from 2001-2002K McGill, D Cowley, L Moran, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 1, 1994
Mutation analysis of coding sequences for type I procollagen in individuals with low bone densityL D Spotila, A Colige, L Sereda, 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.
The Journal of Clinical Investigation|December 1, 1995
Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidismS H Pearce, D Trump, C Wooding, 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.
Pageof 46

Showing results (391-400 of 454) with videos related to

Sort By:
Pageof 46
Bone|May 16, 2019
New explanation for autosomal dominant high bone mass: Mutation of low-density lipoprotein receptor-related protein 6Michael P Whyte, William H McAlister, Fan Zhang, et al.
European Journal of Human Genetics : EJHG|October 8, 2009
Comparison of human chromosome 19q13 and syntenic region on mouse chromosome 7 reveals absence, in man, of 11.6 Mb containing four mouse calcium-sensing receptor-related sequences: relevance to familial benign hypocalciuric hypercalcaemia type 3Fadil M Hannan, M Andrew Nesbit, Jeremy J O Turner, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 31, 2012
Enzyme replacement prevents enamel defects in hypophosphatasia miceManisha C Yadav, Rodrigo Cardoso de Oliveira, Brian L Foster, et al.
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.
Epidemiology and Infection|April 21, 2006
Antibiotic resistance of retail food and human Campylobacter isolates on the island of Ireland from 2001-2002K McGill, D Cowley, L Moran, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 1, 1994
Mutation analysis of coding sequences for type I procollagen in individuals with low bone densityL D Spotila, A Colige, L Sereda, 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.
The Journal of Clinical Investigation|December 1, 1995
Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidismS H Pearce, D Trump, C Wooding, 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.
Pageof 46