Manju Ghosh
New Delhi, DL, India
Last Updated: 09/26/2026
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Found 8 publications
Transethnic analysis of psoriasis susceptibility in South Asians and Europeans enhances fine-mapping in the MHC and genomewide.
Journal: HGG advances
Published: December 20, 2021
Spectrum of GJB2 gene variants in Indian children with non-syndromic hearing loss.
Journal: The Indian journal of medical research
Published: September 01, 2018
Identification of a novel homozygous mutation in transmembrane channel like 1 (TMC1) gene, one of the second-tier hearing loss genes after GJB2 in India.
Journal: The Indian journal of medical research
Published: September 02, 2017
Williams-Beuren Syndrome: Experience of 43 Patients and a Report of an Atypical Case from a Tertiary Care Center in India.
Journal: Cytogenetic and genome research
Published: July 07, 2015
Sequential occurrence of preneoplastic lesions and accumulation of loss of heterozygosity in patients with gallbladder stones suggest causal association with gallbladder cancer.
Journal: Annals of surgery
Published: May 16, 2014
Brachytelephalangic chondrodysplasia punctata: a case series to further delineate the phenotype.
Journal: Clinical dysmorphology
Published: May 15, 2012
Norrie disease: first mutation report and prenatal diagnosis in an Indian family.
Journal: Indian journal of pediatrics
Published: January 25, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026