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Human Mutation|October 12, 2013
Targeted deep resequencing identifies MID2 mutation for X-linked intellectual disability with varied disease severity in a large kindred from IndiaThenral S Geetha, Kulandaimanuvel Antony Michealraj, Madhulika Kabra, et al.
Indian Journal of Medical Ethics|August 20, 2018
Integrating Ethics into the Physiology curriculum: a scale-up study in three medical colleges in Karnataka, South IndiaD Savitha, S Geetha, Suma Bhaskar, et al.
International Journal of Pharmaceutics|February 23, 2025
Advances in metal-organic framework-based drug delivery systemsM T Khulood, U S Jijith, P P Naseef, et al.
Physiology and Molecular Biology of Plants : an International Journal of Functional Plant Biology|February 5, 2015
A maize α-zein promoter drives an endosperm-specific expression of transgene in riceJ Beslin Joshi, S Geetha, Birla Singh, et al.
Clinical Genetics|December 10, 2023
Diagnostic exome identifies a novel PRKG2 mutation in a proband with skeletal dysplasiaPayal Kamdar, Thenral S Geetha, Thomas Palocaren, et al.
Indian Journal of Gastroenterology : Official Journal of the Indian Society of Gastroenterology|November 21, 2015
Clinical profile of PanIN lesions in tropical chronic pancreatitisR S Sindhu, G Parvathy, K Fysal, et al.
Molecular Genetics & Genomic Medicine|December 23, 2017
A novel splice variant in EMC1 is associated with cerebellar atrophy, visual impairment, psychomotor retardation with epilepsyThenral S Geetha, Lokesh Lingappa, Abhishek Ravindra Jain, et al.
Pediatric Nephrology (Berlin, Germany)|October 9, 2020
Phenotypic variability in distal acidification defects associated with WDR72 mutationsPriyanka Khandelwal, Mahesh V, Vijay Prakash Mathur, et al.
Indian Pediatrics|August 27, 2020
Guidelines on Diagnosis and Management of Cow's Milk Protein AllergyJohn Matthai, Malathi Sathiasekharan, Ujjal Poddar, et al.
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