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M J Econs

Showing results (41-50 of 57) with videos related to

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Journal of Musculoskeletal & Neuronal Interactions|December 21, 2007
A homozygous missense mutation in human KLOTHO causes severe tumoral calcinosisS Ichikawa, E A Imel, M L Kreiter, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1994
Fine structure mapping of the human X-linked hypophosphatemic rickets gene locusM J Econs, P S Rowe, F Francis, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|January 25, 2006
Polymorphisms in the bone morphogenetic protein 2 (BMP2) gene do not affect bone mineral density in white men or womenS Ichikawa, M L Johnson, D L Koller, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 1, 1993
Flanking markers define the X-linked hypophosphatemic rickets gene locusM J Econs, P R Fain, M Norman, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|December 17, 2008
Evaluation of vertebral fracture assessment by dual X-ray absorptiometry in a multicenter settingT Fuerst, C Wu, H K Genant, et al.
Bone|June 24, 2000
Sib pair linkage and association studies between bone mineral density and the interleukin-6 gene locusI Takacs, D L Koller, M Peacock, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|October 17, 2007
Effect of raloxifene after recombinant teriparatide [hPTH(1-34)] treatment in postmenopausal women with osteoporosisS Adami, J San Martin, M Muñoz-Torres, et al.
Clinical Genetics|March 19, 2010
Osteoglophonic dysplasia: A 'common' mutation in a rare diseaseA J Sow, R Ramli, Z A Latiff, et al.
The Journal of Clinical Endocrinology and Metabolism|October 13, 1998
A PHEX gene mutation is responsible for adult-onset vitamin D-resistant hypophosphatemic osteomalacia: evidence that the disorder is not a distinct entity from X-linked hypophosphatemic ricketsM J Econs, N E Friedman, P S Rowe, et al.
European Journal of Human Genetics : EJHG|August 10, 1999
Non-random distribution of mutations in the PHEX gene, and under-detected missense mutations at non-conserved residuesD Filisetti, G Ostermann, M von Bredow, et al.
Pageof 6

Showing results (41-50 of 57) with videos related to

Sort By:
Pageof 6
Journal of Musculoskeletal & Neuronal Interactions|December 21, 2007
A homozygous missense mutation in human KLOTHO causes severe tumoral calcinosisS Ichikawa, E A Imel, M L Kreiter, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1994
Fine structure mapping of the human X-linked hypophosphatemic rickets gene locusM J Econs, P S Rowe, F Francis, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|January 25, 2006
Polymorphisms in the bone morphogenetic protein 2 (BMP2) gene do not affect bone mineral density in white men or womenS Ichikawa, M L Johnson, D L Koller, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 1, 1993
Flanking markers define the X-linked hypophosphatemic rickets gene locusM J Econs, P R Fain, M Norman, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|December 17, 2008
Evaluation of vertebral fracture assessment by dual X-ray absorptiometry in a multicenter settingT Fuerst, C Wu, H K Genant, et al.
Bone|June 24, 2000
Sib pair linkage and association studies between bone mineral density and the interleukin-6 gene locusI Takacs, D L Koller, M Peacock, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|October 17, 2007
Effect of raloxifene after recombinant teriparatide [hPTH(1-34)] treatment in postmenopausal women with osteoporosisS Adami, J San Martin, M Muñoz-Torres, et al.
Clinical Genetics|March 19, 2010
Osteoglophonic dysplasia: A 'common' mutation in a rare diseaseA J Sow, R Ramli, Z A Latiff, et al.
The Journal of Clinical Endocrinology and Metabolism|October 13, 1998
A PHEX gene mutation is responsible for adult-onset vitamin D-resistant hypophosphatemic osteomalacia: evidence that the disorder is not a distinct entity from X-linked hypophosphatemic ricketsM J Econs, N E Friedman, P S Rowe, et al.
European Journal of Human Genetics : EJHG|August 10, 1999
Non-random distribution of mutations in the PHEX gene, and under-detected missense mutations at non-conserved residuesD Filisetti, G Ostermann, M von Bredow, et al.
Pageof 6