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Ravi Savarirayan

Showing results (81-90 of 186) with videos related to

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Plos One|October 29, 2020
A community-based co-designed genetic health service model for Aboriginal AustraliansImogen Elsum, Libby Massey, Callum McEwan, et al.
Annals of Plastic Surgery|March 24, 2005
Neuropsychological diversity in Apert syndrome: a comparison of cognitive profilesAnnette C Da Costa, Ravi Savarirayan, Jacquie A Wrennall, et al.
American Journal of Medical Genetics. Part A|June 11, 2015
SNP microarray abnormalities in a cohort of 28 infants with congenital diaphragmatic herniaZornitza Stark, Joanna Behrsin, Trent Burgess, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|October 24, 2007
Bulldog dwarfism in Dexter cattle is caused by mutations in ACANJulie A L Cavanagh, Imke Tammen, Peter A Windsor, et al.
Human Mutation|December 6, 2008
In Vitro studies of non poly alanine PHOX2B mutations argue against a loss-of-function mechanism for congenital central hypoventilationDelphine Trochet, Yves Mathieu, Loïc de Pontual, et al.
Current Rheumatology Reports|December 17, 2013
The collagenopathies: review of clinical phenotypes and molecular correlationsRebekah Jobling, Rohan D'Souza, Naomi Baker, et al.
Journal of Paediatrics and Child Health|February 14, 2019
Diagnostic and service impact of genomic testing technologies in a neonatal intensive care unitNatalie B Tan, Tiong Yang Tan, Melissa M Martyn, et al.
JAMA|October 4, 2007
Effect of perindopril on large artery stiffness and aortic root diameter in patients with Marfan syndrome: a randomized controlled trialAnna A Ahimastos, Anuradha Aggarwal, Kellie M D'Orsa, et al.
American Journal of Medical Genetics. Part A|November 7, 2025
Feeding, Nutrition, and Physical Activity From the Perspectives of People With Skeletal Dysplasia in Australia and Norway: A Mixed Qualitative Methods StudyNatassja Billich, Johanne Kjellevik Ledang, Anne-Mette Bredahl, et al.
Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics|February 2, 2006
Dental findings in a family with hyperparathyroidism-jaw tumor syndrome and a novel HRPT2 gene mutationMichael J Aldred, Anna A Talacko, Ravi Savarirayan, et al.
Pageof 19

Showing results (81-90 of 186) with videos related to

Sort By:
Pageof 19
Plos One|October 29, 2020
A community-based co-designed genetic health service model for Aboriginal AustraliansImogen Elsum, Libby Massey, Callum McEwan, et al.
Annals of Plastic Surgery|March 24, 2005
Neuropsychological diversity in Apert syndrome: a comparison of cognitive profilesAnnette C Da Costa, Ravi Savarirayan, Jacquie A Wrennall, et al.
American Journal of Medical Genetics. Part A|June 11, 2015
SNP microarray abnormalities in a cohort of 28 infants with congenital diaphragmatic herniaZornitza Stark, Joanna Behrsin, Trent Burgess, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|October 24, 2007
Bulldog dwarfism in Dexter cattle is caused by mutations in ACANJulie A L Cavanagh, Imke Tammen, Peter A Windsor, et al.
Human Mutation|December 6, 2008
In Vitro studies of non poly alanine PHOX2B mutations argue against a loss-of-function mechanism for congenital central hypoventilationDelphine Trochet, Yves Mathieu, Loïc de Pontual, et al.
Current Rheumatology Reports|December 17, 2013
The collagenopathies: review of clinical phenotypes and molecular correlationsRebekah Jobling, Rohan D'Souza, Naomi Baker, et al.
Journal of Paediatrics and Child Health|February 14, 2019
Diagnostic and service impact of genomic testing technologies in a neonatal intensive care unitNatalie B Tan, Tiong Yang Tan, Melissa M Martyn, et al.
JAMA|October 4, 2007
Effect of perindopril on large artery stiffness and aortic root diameter in patients with Marfan syndrome: a randomized controlled trialAnna A Ahimastos, Anuradha Aggarwal, Kellie M D'Orsa, et al.
American Journal of Medical Genetics. Part A|November 7, 2025
Feeding, Nutrition, and Physical Activity From the Perspectives of People With Skeletal Dysplasia in Australia and Norway: A Mixed Qualitative Methods StudyNatassja Billich, Johanne Kjellevik Ledang, Anne-Mette Bredahl, et al.
Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics|February 2, 2006
Dental findings in a family with hyperparathyroidism-jaw tumor syndrome and a novel HRPT2 gene mutationMichael J Aldred, Anna A Talacko, Ravi Savarirayan, et al.
Pageof 19