Suchergebnisse - "Ghosh, Manju"

PubPharm (64)

1

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

enthalten in: HGG advances | 2022

von Stuart, P. | Tsoi, L. | Nair, R. | +20

2

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

enthalten in: The Indian journal of medical research | 2018

von Singh, P. | Sharma, S. | Ghosh, M. | +3

3

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

enthalten in: The Indian journal of medical research | 2017

von Singh, P. | Ghosh, M. | Sharma, S. | +5

4

Application of chromosomal microarrays in the evaluation of intellectual disability/global developmental delay patients - A study from a tertiary care genetic centre in India

enthalten in: Gene | 2016

von Gupta, N. | Chowdhury, M. | Sapra, S. | +3

5

Application of chromosomal microarrays in the evaluation of intellectual disability/global developmental delay patients - A study from a tertiary care genetic centre in India

enthalten in: Gene | 2016

von Sharma, P. | Gupta, N. | Chowdhury, M. | +4

6

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

enthalten in: Cytogenetic and genome research | 2015

von Sharma, P. | Gupta, N. | Chowdhury, M. | +5

7

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

enthalten in: Cytogenetic and genome research | 2015

von Sharma, P. | Gupta, N. | Chowdhury, M. | +5

8

Sequential occurrence of preneoplastic lesions and accumulation of loss of heterozygosity in patients with gallbladder stones suggest causal association with gallbladder cancer

enthalten in: Annals of surgery | 2014

von Jain, K. | Mohapatra, T. | Das, P. | +8

CommentIn: Ann Surg. 2016 Mar;263(3):e57. - PMID 25575261

9

TMC1 may be a common gene for nonsyndromic hereditary hearing loss in Indian population

enthalten in: Molecular cytogenetics | 2014

von Singh, P. | Sharma, S. | Ghosh, M. | +4

10

Application of Chromosomal Microarray and Multiplex Ligation-dependent Probe Amplification in prenatal diagnosis

enthalten in: Molecular cytogenetics | 2014

von Sharma, P. | Roy Chowdhury, M. | Gupta, N. | +5

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