Muhammad Bilal

Islamabad, IS, Pakistan

Last Updated: 09/26/2026

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Found 31 publications

HOXD12 a candidate gene for a novel form of synpolydactyly.

HOXD12 a candidate gene for a novel form of synpolydactyly.

Journal: Bone

Published: December 10, 2025

A Novel Variant in the Cyto-Tail of SMO Gene Underlying Isolated Postaxial Polydactyly.

A Novel Variant in the Cyto-Tail of SMO Gene Underlying Isolated Postaxial Polydactyly.

Journal: Molecular syndromology

Published: March 04, 2024

Dynamic interplay of metal and metal oxide nanoparticles with plants: Influencing factors, action mechanisms, and assessment of stimulatory and inhibitory effects.

Dynamic interplay of metal and metal oxide nanoparticles with plants: Influencing factors, action mechanisms, and assessment of stimulatory and inhibitory effects.

Journal: Ecotoxicology and environmental safety

Published: September 09, 2023

Sequence variants in different genes underlying Bardet-Biedl syndrome in four consanguineous families.

Sequence variants in different genes underlying Bardet-Biedl syndrome in four consanguineous families.

Journal: Molecular biology reports

Published: June 19, 2023

Variants in EFCAB7 underlie nonsyndromic postaxial polydactyly.

Variants in EFCAB7 underlie nonsyndromic postaxial polydactyly.

Journal: European journal of human genetics : EJHG

Published: April 28, 2023

De novo missense variants in phosphatidylinositol kinase PIP5KIγ underlie a neurodevelopmental syndrome associated with altered phosphoinositide signaling.

De novo missense variants in phosphatidylinositol kinase PIP5KIγ underlie a neurodevelopmental syndrome associated with altered phosphoinositide signaling.

Journal: American journal of human genetics

Published: January 24, 2023

Indole-3-acetic acid (IAA) doping on the surface of CuO-NPs reduces the toxic effects of NPs on Lactuca sativa.

Indole-3-acetic acid (IAA) doping on the surface of CuO-NPs reduces the toxic effects of NPs on Lactuca sativa.

Journal: Journal of biotechnology

Published: December 20, 2022

Case report: A novel de novo loss of function variant in the DNA-binding domain of TBX2 causes severe osteochondrodysplasia.

Case report: A novel de novo loss of function variant in the DNA-binding domain of TBX2 causes severe osteochondrodysplasia.

Journal: Frontiers in genetics

Published: December 06, 2022

Homozygous Missense Variant in the Solute Carrier Organic Anion Transporter 2A1 (SLCO2A1) Gene Underlies Isolated Nail Clubbing.

Homozygous Missense Variant in the Solute Carrier Organic Anion Transporter 2A1 (SLCO2A1) Gene Underlies Isolated Nail Clubbing.

Journal: Genes

Published: November 22, 2022

Sequence Variants in MEGF8 and GJA1 Underlying Syndactyly.

Sequence Variants in MEGF8 and GJA1 Underlying Syndactyly.

Journal: Molecular syndromology

Published: August 03, 2022

Genetic overview of postaxial polydactyly: Updated classification.

Genetic overview of postaxial polydactyly: Updated classification.

Journal: Clinical genetics

Published: July 21, 2022

A novel biallelic variant further delineates PRDX3-related autosomal recessive cerebellar ataxia.

A novel biallelic variant further delineates PRDX3-related autosomal recessive cerebellar ataxia.

Journal: Neurogenetics

Published: July 18, 2022

Showing 1-12 of 31

Last Updated: 09/26/2026