Anjana Kar
Hyderabad, TG, India
Last Updated: 09/26/2026
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Found 9 publications
Expanding the Phenotypic Spectrum of Syndromic Arthrogryposis Multiplex Congenita: Role of Biallelic Variants in COL25A1 Across Fetal and Pediatric Periods.
Journal: Indian journal of pediatrics
Published: July 30, 2025
A Novel Variant c.149G>A in CDK5 Gene Causing Lissencephaly Type 7.
Journal: Clinical genetics
Published: March 03, 2025
A Novel FGFR1 Mutation Causing Familial Normosmic Hypogonadotropic Hypogonadism in Three Sisters.
Journal: Journal of obstetrics and gynaecology of India
Published: March 13, 2024
Rare genetic diseases in India: Steps toward a nationwide mission program.
Journal: Journal of biosciences
Published: February 22, 2024
Epigenetic interaction of microbes with their mammalian hosts.
Journal: Journal of biosciences
Published: November 03, 2021
Whole exome sequencing reveals a mutation in ARMC9 as a cause of mental retardation, ptosis, and polydactyly.
Journal: American journal of medical genetics. Part A
Published: June 03, 2017
Complex Camptosynpolydactyly and Mesoaxial synostotic syndactyly with phalangeal reduction are allelic disorders.
Journal: American journal of medical genetics. Part A
Published: December 22, 2015
Identification of Promotor and Exonic Variations, and Functional Characterization of a Splice Site Mutation in Indian Patients with Unconjugated Hyperbilirubinemia.
Journal: PloS one
Published: October 21, 2015
Showing 1-9 of 9
Last Updated: 09/26/2026