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Ishwar Chander Verma

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Journal of Human Genetics|March 1, 2019

Identification of PKD1 and PKD2 gene variants in a cohort of 125 Asian Indian patients of ADPKDShewata Pandita, Vijaya Ramachandran, Prahlad Balakrishnan, et al.

Annals of Human Genetics|May 19, 2018

Clinical and molecular characterization of Indian patients with fructose-1, 6-bisphosphatase deficiency: Identification of a frequent variant (E281K)Pratibha Bhai, Sunita Bijarnia-Mahay, Ratna D Puri, et al.

JIMD Reports|November 18, 2020

Fabry disease in India: A multicenter study of the clinical and mutation spectrum in 54 patientsSheela Nampoothiri, Dhanya Yesodharan, Amrita Bhattacherjee, et al.

Journal of Obstetrics and Gynaecology of India|November 13, 2018

Single Nucleotide Polymorphism-Based Noninvasive Prenatal Testing: Experience in IndiaIshwar Chander Verma, Ratna Puri, Eswarachary Venkataswamy, et al.

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Search research articles

Showing results (31-40 of 34) with videos related to

Sort By:

Pageof 4

You have reached the last page of results.This site can display upto 34 results.

Journal of Human Genetics|March 1, 2019

Identification of PKD1 and PKD2 gene variants in a cohort of 125 Asian Indian patients of ADPKDShewata Pandita, Vijaya Ramachandran, Prahlad Balakrishnan, et al.

Annals of Human Genetics|May 19, 2018

JIMD Reports|November 18, 2020

Fabry disease in India: A multicenter study of the clinical and mutation spectrum in 54 patientsSheela Nampoothiri, Dhanya Yesodharan, Amrita Bhattacherjee, et al.

Journal of Obstetrics and Gynaecology of India|November 13, 2018

Single Nucleotide Polymorphism-Based Noninvasive Prenatal Testing: Experience in IndiaIshwar Chander Verma, Ratna Puri, Eswarachary Venkataswamy, et al.

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