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Journal of Medical Genetics|December 8, 2011
Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashionEva Klopocki, Silke Lohan, Sandra C Doelken, et al.European Journal of Human Genetics : EJHG|December 20, 2024
Genetic and allelic heterogeneity in 248 Indians with skeletal dysplasiaPrince Jacob, Swati Singh, Gandham SriLakshmi Bhavani, et al.Journal of Pediatric Orthopedics|February 4, 2025
An International Consensus on Evaluation and Management of Idiopathic Genu Valgum: A Modified Delphi SurveyAshish S Ranade, Gauri A Oka, Mohan V Belthur, et al.American Journal of Medical Genetics. Part A|September 25, 2014
GALNS mutations in Indian patients with mucopolysaccharidosis IVAAbdul Mueed Bidchol, Ashwin Dalal, Hitesh Shah, et al.Clinical Genetics|July 24, 2021
Clinical and genetic spectrum of 104 Indian families with central nervous system white matter abnormalitiesParneet Kaur, Michelle C do Rosario, Malavika Hebbar, et al.Gene|May 5, 2015
Recurrent and novel GLB1 mutations in IndiaAbdul Mueed Bidchol, Ashwin Dalal, Rakesh Trivedi, et al.The Bone & Joint Journal|May 31, 2026
Femoral nerve palsy in brace treatment for developmental dysplasia of the hip : incidence and outcomes in a prospective international cohortEmily K Schaeffer, Alice Wei Ting Wang, Jack Hu, et al.BMJ Open|August 24, 2023
Safer medicines To reduce falls and refractures for OsteoPorosis (#STOP): a study protocol for a randomised controlled trial of medical specialist-initiated pharmacist-led medication management reviews in primary careRebekah Jane Moles, Lin Perry, Justine M Naylor, et al.The Journal of the Association of Physicians of India|June 24, 2025
Expert Consensus on Lifestyle Modifications in Hypertension Management: An Indian PerspectiveJagdish Hiremath, Gurpreet S Wander, Arup Dasbiswas, et al.Pageof 19