Abdul M. Bidchol

Manipala, KA, India

Last Updated: 09/26/2026

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Found 8 publications

Phenotype and genotype in patients with Larsen syndrome: clinical homogeneity and allelic heterogeneity in seven patients.

Phenotype and genotype in patients with Larsen syndrome: clinical homogeneity and allelic heterogeneity in seven patients.

Journal: BMC medical genetics

Published: August 14, 2015

Recurrent and novel GLB1 mutations in India.

Recurrent and novel GLB1 mutations in India.

Journal: Gene

Published: March 23, 2015

White matter changes in GM1 gangliosidosis.

White matter changes in GM1 gangliosidosis.

Journal: Indian pediatrics

Published: February 19, 2015

GALNS mutations in Indian patients with mucopolysaccharidosis IVA.

GALNS mutations in Indian patients with mucopolysaccharidosis IVA.

Journal: American journal of medical genetics. Part A

Published: October 26, 2013

A novel frameshift mutation in TWIST2 gene causing Setleis syndrome.

A novel frameshift mutation in TWIST2 gene causing Setleis syndrome.

Journal: Indian journal of pediatrics

Published: August 01, 2013

A novel mutation (g.106737G>T) in zone of polarizing activity regulatory sequence (ZRS) causes variable limb phenotypes in Werner mesomelia.

A novel mutation (g.106737G>T) in zone of polarizing activity regulatory sequence (ZRS) causes variable limb phenotypes in Werner mesomelia.

Journal: American journal of medical genetics. Part A

Published: July 05, 2013

Novel mutation in an Indian patient with Methylmalonic Acidemia, cblA type.

Novel mutation in an Indian patient with Methylmalonic Acidemia, cblA type.

Journal: Indian journal of human genetics

Published: May 30, 2013

Analysis of the WISP3 gene in Indian families with progressive pseudorheumatoid dysplasia.

Analysis of the WISP3 gene in Indian families with progressive pseudorheumatoid dysplasia.

Journal: American journal of medical genetics. Part A

Published: May 02, 2012

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Last Updated: 09/26/2026