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Abdul Mueed Bidchol

Showing results (1-10 of 9) with videos related to

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Indian Pediatrics|February 19, 2015
White matter changes in GM1 gangliosidosisMoni Tuteja, Abdul Mueed Bidchol, Katta Mohan Girisha, et al.
Indian Journal of Pediatrics|October 16, 2013
A novel frameshift mutation in TWIST2 gene causing Setleis syndromeKatta Mohan Girisha, Abdul Mueed Bidchol, Murali Keshava Sarpangala, et al.
Indian Journal of Human Genetics|May 30, 2013
Novel mutation in an Indian patient with Methylmalonic Acidemia, cblA typeKatta Mohan Girisha, Aroor Shrikiran, Abdul Mueed Bidchol, 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.
BMC Medical Genetics|April 7, 2016
Phenotype and genotype in patients with Larsen syndrome: clinical homogeneity and allelic heterogeneity in seven patientsKatta Mohan Girisha, Abdul Mueed Bidchol, Luitgard Graul-Neumann, et al.
Molecular Syndromology|October 23, 2014
Exome Sequencing Identifies a Dominant TNNT3 Mutation in a Large Family with Distal ArthrogryposisSarah B Daly, Hitesh Shah, James O'Sullivan, 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.
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.
Gene|May 5, 2015
Recurrent and novel GLB1 mutations in IndiaAbdul Mueed Bidchol, Ashwin Dalal, Rakesh Trivedi, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Indian Pediatrics|February 19, 2015
White matter changes in GM1 gangliosidosisMoni Tuteja, Abdul Mueed Bidchol, Katta Mohan Girisha, et al.
Indian Journal of Pediatrics|October 16, 2013
A novel frameshift mutation in TWIST2 gene causing Setleis syndromeKatta Mohan Girisha, Abdul Mueed Bidchol, Murali Keshava Sarpangala, et al.
Indian Journal of Human Genetics|May 30, 2013
Novel mutation in an Indian patient with Methylmalonic Acidemia, cblA typeKatta Mohan Girisha, Aroor Shrikiran, Abdul Mueed Bidchol, 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.
BMC Medical Genetics|April 7, 2016
Phenotype and genotype in patients with Larsen syndrome: clinical homogeneity and allelic heterogeneity in seven patientsKatta Mohan Girisha, Abdul Mueed Bidchol, Luitgard Graul-Neumann, et al.
Molecular Syndromology|October 23, 2014
Exome Sequencing Identifies a Dominant TNNT3 Mutation in a Large Family with Distal ArthrogryposisSarah B Daly, Hitesh Shah, James O'Sullivan, 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.
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.
Gene|May 5, 2015
Recurrent and novel GLB1 mutations in IndiaAbdul Mueed Bidchol, Ashwin Dalal, Rakesh Trivedi, et al.
Pageof 1