Amjad Khan

P.R. China
Shenyang, 110122, China

Last Updated: 09/26/2026

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Found 18 publications

Retraction Note: Forensic characterization of 15 autosomal STRs in four populations from Xinjiang, China, and genetic relationships with neighboring populations.

Retraction Note: Forensic characterization of 15 autosomal STRs in four populations from Xinjiang, China, and genetic relationships with neighboring populations.

Journal: Scientific reports

Published: June 17, 2024

Author Correction: Forensic characterization of 15 autosomal STRs in four populations from Xinjiang, China, and genetic relationships with neighboring populations.

Author Correction: Forensic characterization of 15 autosomal STRs in four populations from Xinjiang, China, and genetic relationships with neighboring populations.

Journal: Scientific reports

Published: July 13, 2022

Phenotypic Characterization of Intellectual Disability Caused by MBOAT7 Mutation in Two Consanguineous Pakistani Families.

Phenotypic Characterization of Intellectual Disability Caused by MBOAT7 Mutation in Two Consanguineous Pakistani Families.

Journal: Frontiers in pediatrics

Published: July 19, 2020

Withdrawal Notice: Electro-Catalytic process for the Synthesis of Organic Compounds and their Biological Applications

Withdrawal Notice: Electro-Catalytic process for the Synthesis of Organic Compounds and their Biological Applications

Journal: Current organic synthesis

Published: June 25, 2020

Homozygous truncating NEK10 mutation, associated with primary ciliary dyskinesia: a case report.

Homozygous truncating NEK10 mutation, associated with primary ciliary dyskinesia: a case report.

Journal: BMC pulmonary medicine

Published: January 16, 2020

NCKAP1L defects lead to a novel syndrome combining immunodeficiency, lymphoproliferation, and hyperinflammation.

NCKAP1L defects lead to a novel syndrome combining immunodeficiency, lymphoproliferation, and hyperinflammation.

Journal: The Journal of experimental medicine

Published: December 03, 2019

A novel DLL4 missense mutation in a Chinese patient with Adams-Oliver syndrome.

A novel DLL4 missense mutation in a Chinese patient with Adams-Oliver syndrome.

Journal: Chinese medical journal

Published: July 02, 2019

A Novel Homozygous Nonsense Mutation p.Cys366* in the WNT10B Gene Underlying Split-Hand/Split Foot Malformation in a Consanguineous Pakistani Family.

A Novel Homozygous Nonsense Mutation p.Cys366* in the WNT10B Gene Underlying Split-Hand/Split Foot Malformation in a Consanguineous Pakistani Family.

Journal: Frontiers in pediatrics

Published: June 11, 2019

Biallelic Missense Mutation in the ECEL1 Underlies Distal Arthrogryposis Type 5 (DA5D).

Biallelic Missense Mutation in the ECEL1 Underlies Distal Arthrogryposis Type 5 (DA5D).

Journal: Frontiers in pediatrics

Published: April 14, 2019

Sequence variants in genes causing nonsyndromic hearing loss in a Pakistani cohort.

Sequence variants in genes causing nonsyndromic hearing loss in a Pakistani cohort.

Journal: Molecular genetics & genomic medicine

Published: February 25, 2019

Use of Pharmacogenetic Drugs by the Dutch Population.

Use of Pharmacogenetic Drugs by the Dutch Population.

Journal: Frontiers in genetics

Published: January 14, 2019

Enhanced antimicrobial, anti-oxidant applications of green synthesized AgNPs- an acute chronic toxicity study of phenolic azo dyes & study of materials surface using X-ray photoelectron spectroscopy.

Enhanced antimicrobial, anti-oxidant applications of green synthesized AgNPs- an acute chronic toxicity study of phenolic azo dyes & study of materials surface using X-ray photoelectron spectroscopy.

Journal: Journal of photochemistry and photobiology. B, Biology

Published: January 09, 2018

Showing 1-12 of 18

Last Updated: 09/26/2026