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Ravi Savarirayan

Showing results (71-80 of 186) with videos related to

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Arthritis and Rheumatism|February 5, 2010
Premature arthritis is a distinct type II collagen phenotypePeter Kannu, John F Bateman, Susan Randle, et al.
Translational Vision Science & Technology|March 2, 2016
Ethical Considerations for the Return of Incidental Findings in Ophthalmic Genomic ResearchEmmanuelle Souzeau, Kathryn P Burdon, David A Mackey, et al.
International Journal for Equity in Health|March 2, 2021
Culturally competent communication in Indigenous disability assessment: a qualitative studyAngeline Ferdinand, Libby Massey, Jennifer Cullen, et al.
International Journal for Equity in Health|April 18, 2021
"This is my boy's health! Talk straight to me!" perspectives on accessible and culturally safe care among Aboriginal and Torres Strait Islander patients of clinical genetics servicesPhilippa Dalach, Ravi Savarirayan, Gareth Baynam, et al.
Orphanet Journal of Rare Diseases|April 8, 2021
Obstructive sleep apnea in Norwegian adults with achondroplasia: a population-based studySvein O Fredwall, Britt Øverland, Hanne Berdal, et al.
Journal of the Endocrine Society|March 5, 2026
Effect of vosoritide on spine morphology in children with achondroplasia: 1-year results from a randomized phase 2 studyMelita Irving, Ravi Savarirayan, Julie E Hoover-Fong, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 14, 2012
TRPV4-associated skeletal dysplasiasGen Nishimura, Ekkehart Lausch, Ravi Savarirayan, et al.
American Journal of Medical Genetics. Part A|July 2, 2003
Somatic and germline mosaicism for a R248C missense mutation in FGFR3, resulting in a skeletal dysplasia distinct from thanatophoric dysplasiaValentine J Hyland, Stephen P Robertson, Simon Flanagan, et al.
Neurosurgery Clinics of North America|November 21, 2021
Multidisciplinary Care of Neurosurgical Patients with Genetic SyndromesMelissa A Villegas, Ericka Okenfuss, Ravi Savarirayan, et al.
American Journal of Medical Genetics. Part A|May 12, 2005
Autosomal recessive omodysplasia: early prenatal diagnosis and a possible clue to the gene locationTiong Yang Tan, George McGillivray, Louise Kornman, et al.
Pageof 19

Showing results (71-80 of 186) with videos related to

Sort By:
Pageof 19
Arthritis and Rheumatism|February 5, 2010
Premature arthritis is a distinct type II collagen phenotypePeter Kannu, John F Bateman, Susan Randle, et al.
Translational Vision Science & Technology|March 2, 2016
Ethical Considerations for the Return of Incidental Findings in Ophthalmic Genomic ResearchEmmanuelle Souzeau, Kathryn P Burdon, David A Mackey, et al.
International Journal for Equity in Health|March 2, 2021
Culturally competent communication in Indigenous disability assessment: a qualitative studyAngeline Ferdinand, Libby Massey, Jennifer Cullen, et al.
International Journal for Equity in Health|April 18, 2021
"This is my boy's health! Talk straight to me!" perspectives on accessible and culturally safe care among Aboriginal and Torres Strait Islander patients of clinical genetics servicesPhilippa Dalach, Ravi Savarirayan, Gareth Baynam, et al.
Orphanet Journal of Rare Diseases|April 8, 2021
Obstructive sleep apnea in Norwegian adults with achondroplasia: a population-based studySvein O Fredwall, Britt Øverland, Hanne Berdal, et al.
Journal of the Endocrine Society|March 5, 2026
Effect of vosoritide on spine morphology in children with achondroplasia: 1-year results from a randomized phase 2 studyMelita Irving, Ravi Savarirayan, Julie E Hoover-Fong, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 14, 2012
TRPV4-associated skeletal dysplasiasGen Nishimura, Ekkehart Lausch, Ravi Savarirayan, et al.
American Journal of Medical Genetics. Part A|July 2, 2003
Somatic and germline mosaicism for a R248C missense mutation in FGFR3, resulting in a skeletal dysplasia distinct from thanatophoric dysplasiaValentine J Hyland, Stephen P Robertson, Simon Flanagan, et al.
Neurosurgery Clinics of North America|November 21, 2021
Multidisciplinary Care of Neurosurgical Patients with Genetic SyndromesMelissa A Villegas, Ericka Okenfuss, Ravi Savarirayan, et al.
American Journal of Medical Genetics. Part A|May 12, 2005
Autosomal recessive omodysplasia: early prenatal diagnosis and a possible clue to the gene locationTiong Yang Tan, George McGillivray, Louise Kornman, et al.
Pageof 19