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European Journal of Medical Genetics|December 3, 2014
Mutations in patients with osteogenesis imperfecta from consanguineous Indian familiesJoshi Stephen, Katta Mohan Girisha, Ashwin Dalal, et al.
American Journal of Medical Genetics. Part A|January 31, 2014
A novel mutation (g.106737G>T) in zone of polarizing activity regulatory sequence (ZRS) causes variable limb phenotypes in Werner mesomeliaKatta M Girisha, Abdul Mueed Bidchol, Preeti S Kamath, et al.
Surgical Neurology International|November 3, 2022
Laminectomy as treatment for abrupt neurological decline in acrodysostosis: A case reportBenjamin Joseph Lee, Lance Villeneuve, Michael Martin
Journal of Pediatric Orthopedics|August 26, 2006
Evaluation of outcome of treatment of congenital clubfootSandeep Munshi, Renjit A Varghese, Benjamin Joseph
Journal of Human Genetics|December 16, 2022
Genome sequencing identifies a large non-coding region deletion of SNX10 causing autosomal recessive osteopetrosisPrajna Udupa, Debasish Kumar Ghosh, Neethukrishna Kausthubham, et al.
American Journal of Medical Genetics. Part A|November 23, 2019
Biallelic variants p.Arg1133Cys and p.Arg1379Cys in COL2A1: Further delineation of phenotypic spectrum of recessive Type 2 collagenopathiesKatta M Girisha, Gandham S Bhavani, Hitesh Shah, et al.
Journal of Pediatric Orthopedics. Part B|April 3, 2009
Congenital posteromedial bowing of the tibia: a retrospective analysis of growth abnormalities in the legHitesh H Shah, Siddesh N Doddabasappa, Benjamin Joseph
The Journal of Laryngology and Otology|December 9, 2025
Tramadol for treatment of neurogenic cough: a retrospective case seriesBenjamin Joseph Rubinstein, Sheela Saidha, John Todd Sinacori
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