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D Grinberg

Showing results (51-60 of 60) with videos related to

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Human Genetics|June 1, 1997
Putative association of a mutant ROM1 allele with retinitis pigmentosaA Martínez-Mir, C Vilela, M Bayés, 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|February 6, 2025
Identifying rare variants in genes related to bone phenotypes in a cohort of postmenopausal womenJ D Patiño-Salazar, D Ovejero, M Gabernet, 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 6, 2006
COL1A1, ESR1, VDR and TGFB1 polymorphisms and haplotypes in relation to BMD in Spanish postmenopausal womenM Bustamante, X Nogués, A Enjuanes, 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|August 27, 2017
Discrepancy between bone density and bone material strength index in three siblings with Camurati-Engelmann diseaseS Herrera, R Soriano, X Nogués, et al.
Scientific Reports|September 19, 2014
A broad spectrum of genomic changes in latinamerican patients with EXT1/EXT2-CDGM A Delgado, G Martinez-Domenech, P Sarrión, 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|May 14, 2009
Polymorphisms and haplotypes across the osteoprotegerin gene associated with bone mineral density and osteoporotic fracturesS Jurado, X Nogués, L Agueda, et al.
Anales Espanoles De Pediatria|June 4, 2002
[Hyperhomocystinemia and 677C T methylenetetrahydrofolate reductase polymorphism as a cardiovascular risk factor in childhood]C Mainou Cid, N García Giralt, M A Vilaseca Buscà, et al.
Scientific Reports|February 27, 2013
Mutations in the EXT1 and EXT2 genes in Spanish patients with multiple osteochondromasP Sarrión, A Sangorrin, R Urreizti, et al.
Journal of Medical Genetics|March 21, 1998
A new autosomal recessive retinitis pigmentosa locus maps on chromosome 2q31-q33M Bayés, B Goldaracena, A Martínez-Mir, et al.
Clinical Genetics|March 19, 2010
Molecular characterization of five patients with homocystinuria due to severe methylenetetrahydrofolate reductase deficiencyR Urreizti, A A Moya-García, A Pino-Ángeles, et al.
Pageof 6

Showing results (51-60 of 60) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 60 results.
Human Genetics|June 1, 1997
Putative association of a mutant ROM1 allele with retinitis pigmentosaA Martínez-Mir, C Vilela, M Bayés, 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|February 6, 2025
Identifying rare variants in genes related to bone phenotypes in a cohort of postmenopausal womenJ D Patiño-Salazar, D Ovejero, M Gabernet, 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 6, 2006
COL1A1, ESR1, VDR and TGFB1 polymorphisms and haplotypes in relation to BMD in Spanish postmenopausal womenM Bustamante, X Nogués, A Enjuanes, 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|August 27, 2017
Discrepancy between bone density and bone material strength index in three siblings with Camurati-Engelmann diseaseS Herrera, R Soriano, X Nogués, et al.
Scientific Reports|September 19, 2014
A broad spectrum of genomic changes in latinamerican patients with EXT1/EXT2-CDGM A Delgado, G Martinez-Domenech, P Sarrión, 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|May 14, 2009
Polymorphisms and haplotypes across the osteoprotegerin gene associated with bone mineral density and osteoporotic fracturesS Jurado, X Nogués, L Agueda, et al.
Anales Espanoles De Pediatria|June 4, 2002
[Hyperhomocystinemia and 677C T methylenetetrahydrofolate reductase polymorphism as a cardiovascular risk factor in childhood]C Mainou Cid, N García Giralt, M A Vilaseca Buscà, et al.
Scientific Reports|February 27, 2013
Mutations in the EXT1 and EXT2 genes in Spanish patients with multiple osteochondromasP Sarrión, A Sangorrin, R Urreizti, et al.
Journal of Medical Genetics|March 21, 1998
A new autosomal recessive retinitis pigmentosa locus maps on chromosome 2q31-q33M Bayés, B Goldaracena, A Martínez-Mir, et al.
Clinical Genetics|March 19, 2010
Molecular characterization of five patients with homocystinuria due to severe methylenetetrahydrofolate reductase deficiencyR Urreizti, A A Moya-García, A Pino-Ángeles, et al.
Pageof 6