Ghosh M - Search Results

1

Transethnic analysis of psoriasis susceptibility in South Asians and Europeans enhances fine-mapping in the MHC and genomewide.

Stuart PE, Tsoi LC, Nair RP, Ghosh M, Kabra M, Shaiq PA, Raja GK, Qamar R, Thelma BK, Patrick MT, Parihar A, Singh S, Khandpur S, Kumar U, Wittig M, Degenhardt F, Tejasvi T, Voorhees JJ, Weidinger S, Franke A, Abecasis GR, Sharma VK, Elder JT. Stuart PE, et al. Among authors: ghosh m. HGG Adv. 2022 Jan 13;3(1):100069. doi: 10.1016/j.xhgg.2021.100069. Epub 2021 Nov 6. HGG Adv. 2022. PMID: 34927100 Free PMC article.

2

Genetics of deafness in India.

Ghosh M, Vijaya R, Kabra M. Ghosh M, et al. Indian J Pediatr. 2004 Jun;71(6):531-3. doi: 10.1007/BF02724296. Indian J Pediatr. 2004. PMID: 15226564

3

Spectrum of GJB2 gene variants in Indian children with non-syndromic hearing loss.

Singh PK, Sharma S, Ghosh M, Shastri SS, Gupta N, Kabra M. Singh PK, et al. Among authors: ghosh m. Indian J Med Res. 2018 Jun;147(6):615-618. doi: 10.4103/ijmr.IJMR_76_16. Indian J Med Res. 2018. PMID: 30168495 Free PMC article. No abstract available.

4

Brachytelephalangic chondrodysplasia punctata: a case series to further delineate the phenotype.

Gupta N, Ghosh M, Shukla R, Das GP, Kabra M. Gupta N, et al. Among authors: ghosh m. Clin Dysmorphol. 2012 Jul;21(3):113-117. doi: 10.1097/MCD.0b013e32835439cd. Clin Dysmorphol. 2012. PMID: 22581171

5

Fraser-cryptophthalmos syndrome.

Kabra M, Gulati S, Ghosh M, Menon PS. Kabra M, et al. Among authors: ghosh m. Indian J Pediatr. 2000 Oct;67(10):775-8. doi: 10.1007/BF02723939. Indian J Pediatr. 2000. PMID: 11105430 Review.

6

A novel MECP2 change in an indian boy with variant rett phenotype and congenital blindness: implications for genetic counseling and prenatal diagnosis.

Khajuria R, Gupta N, Sapra S, Gulati S, Ghosh M, Kalra V, Kabra M. Khajuria R, et al. Among authors: ghosh m. J Child Neurol. 2011 Feb;26(2):209-13. doi: 10.1177/0883073810378535. J Child Neurol. 2011. PMID: 21285040

7

Williams-Beuren Syndrome: Experience of 43 Patients and a Report of an Atypical Case from a Tertiary Care Center in India.

Sharma P, Gupta N, Chowdhury MR, Phadke SR, Sapra S, Halder A, Ghosh M, Kabra M. Sharma P, et al. Among authors: ghosh m. Cytogenet Genome Res. 2015;146(3):187-94. doi: 10.1159/000439205. Epub 2015 Sep 10. Cytogenet Genome Res. 2015. PMID: 26352091

8

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.

Singh PK, Ghosh M, Sharma S, Shastri S, Gupta N, Chowdhury MR, Anand A, Kabra M. Singh PK, et al. Among authors: ghosh m. Indian J Med Res. 2017 Apr;145(4):492-497. doi: 10.4103/ijmr.IJMR_397_15. Indian J Med Res. 2017. PMID: 28862181 Free PMC article.

9

Cystic fibrosis--an Indian perspective on recent advances in diagnosis and management.

Kabra SK, Kabra M, Ghosh M, Verma IC. Kabra SK, et al. Among authors: ghosh m. Indian J Pediatr. 1996 Mar-Apr;63(2):189-98. doi: 10.1007/BF02845243. Indian J Pediatr. 1996. PMID: 10829988 Review.

10

Idiopathic cranio-osteoarthropathy.

Kabra M, Kabra SK, Ghosh M, Gupta AK, Menon PS. Kabra M, et al. Among authors: ghosh m. Indian Pediatr. 2000 Jun;37(6):659-62. Indian Pediatr. 2000. PMID: 10869149 No abstract available.

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