K M Girisha - JoVE Visualize

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Indian Journal of Medical Sciences|April 5, 2005

TNFR2 gene polymorphism in coronary artery diseaseV H Sankar, K M Girisha, A Gilmour, et al.

Indian Journal of Medical Sciences|January 4, 2005

T1 and M1 polymorphism in glutathione S-transferase gene and coronary artery disease in North Indian populationK M Girisha, A Gilmour, S Mastana, et al.

Genetic Counseling (Geneva, Switzerland)|September 19, 2018

EVALUATION OF MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION AS A TOOL FOR DIAGNOSIS AND CARRIER DETECTION IN FAMILIES WITH A DYSTROPHINOPATHYS Salian, S A Vahab, H Shah, et al.

BMC Medical Genetics|December 13, 2007

Synpolydactyly and HOXD13 polyalanine repeat: addition of 2 alanine residues is without clinical consequencesSajid Malik, K M Girisha, Muhammad Wajid, et al.

Clinical Genetics|March 23, 2018

Seven additional families with spondylocarpotarsal synostosis syndrome with novel biallelic deleterious variants in FLNBS Salian, A Shukla, H Shah, et al.

Journal of Applied Genetics|February 11, 2010

Rhizomelic chondrodysplasia punctata type 1: report of mutations in 3 children from IndiaS R Phadke, N Gupta, K M Girisha, et al.

Clinical Genetics|January 25, 2014

Microduplications encompassing the Sonic hedgehog limb enhancer ZRS are associated with Haas-type polysyndactyly and Laurin-Sandrow syndromeS Lohan, M Spielmann, S C Doelken, et al.

American Journal of Medical Genetics. Part A|September 19, 2012

Analysis of the WISP3 gene in Indian families with progressive pseudorheumatoid dysplasiaAshwin Dalal, Sri Lakshmi Bhavani G, Padma Priya Togarrati, et al.

Journal of the European Academy of Dermatology and Venereology : JEADV|May 11, 2022

Biallelic KITLG variants lead to a distinct spectrum of hypomelanosis and sensorineural hearing lossB Vona, D A Schwartzbaum, A A Rodriguez, et al.

Clinical Genetics|May 6, 2016

Identification and characterization of 20 novel pathogenic variants in 60 unrelated Indian patients with mucopolysaccharidoses type I and type IIA Uttarilli, P Ranganath, D Matta, et al.

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Showing results (31-40 of 42) with videos related to

Sort By:

Pageof 5

Indian Journal of Medical Sciences|April 5, 2005

TNFR2 gene polymorphism in coronary artery diseaseV H Sankar, K M Girisha, A Gilmour, et al.

Indian Journal of Medical Sciences|January 4, 2005

T1 and M1 polymorphism in glutathione S-transferase gene and coronary artery disease in North Indian populationK M Girisha, A Gilmour, S Mastana, et al.

Genetic Counseling (Geneva, Switzerland)|September 19, 2018

EVALUATION OF MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION AS A TOOL FOR DIAGNOSIS AND CARRIER DETECTION IN FAMILIES WITH A DYSTROPHINOPATHYS Salian, S A Vahab, H Shah, et al.

BMC Medical Genetics|December 13, 2007

Synpolydactyly and HOXD13 polyalanine repeat: addition of 2 alanine residues is without clinical consequencesSajid Malik, K M Girisha, Muhammad Wajid, et al.

Clinical Genetics|March 23, 2018

Seven additional families with spondylocarpotarsal synostosis syndrome with novel biallelic deleterious variants in FLNBS Salian, A Shukla, H Shah, et al.

Journal of Applied Genetics|February 11, 2010

Rhizomelic chondrodysplasia punctata type 1: report of mutations in 3 children from IndiaS R Phadke, N Gupta, K M Girisha, et al.

Clinical Genetics|January 25, 2014

Microduplications encompassing the Sonic hedgehog limb enhancer ZRS are associated with Haas-type polysyndactyly and Laurin-Sandrow syndromeS Lohan, M Spielmann, S C Doelken, et al.

American Journal of Medical Genetics. Part A|September 19, 2012

Analysis of the WISP3 gene in Indian families with progressive pseudorheumatoid dysplasiaAshwin Dalal, Sri Lakshmi Bhavani G, Padma Priya Togarrati, et al.

Journal of the European Academy of Dermatology and Venereology : JEADV|May 11, 2022

Biallelic KITLG variants lead to a distinct spectrum of hypomelanosis and sensorineural hearing lossB Vona, D A Schwartzbaum, A A Rodriguez, et al.

Clinical Genetics|May 6, 2016

Identification and characterization of 20 novel pathogenic variants in 60 unrelated Indian patients with mucopolysaccharidoses type I and type IIA Uttarilli, P Ranganath, D Matta, et al.

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