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Implications in disclosing auditory genetic mutation to a family: a case study.
Int J Audiol. 2007 Jul;46(7):384-7. doi: 10.1080/14992020701297805.
Int J Audiol. 2007.
PMID: 17680470
Functional consequences of novel connexin 26 mutations associated with hereditary hearing loss.
Mani RS, Ganapathy A, Jalvi R, Srikumari Srisailapathy CR, Malhotra V, Chadha S, Agarwal A, Ramesh A, Rangasayee RR, Anand A.
Mani RS, et al. Among authors: jalvi r.
Eur J Hum Genet. 2009 Apr;17(4):502-9. doi: 10.1038/ejhg.2008.179. Epub 2008 Oct 22.
Eur J Hum Genet. 2009.
PMID: 18941476
Free PMC article.
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Non-syndromic hearing impairment in India: high allelic heterogeneity among mutations in TMPRSS3, TMC1, USHIC, CDH23 and TMIE.
Ganapathy A, Pandey N, Srisailapathy CR, Jalvi R, Malhotra V, Venkatappa M, Chatterjee A, Sharma M, Santhanam R, Chadha S, Ramesh A, Agarwal AK, Rangasayee RR, Anand A.
Ganapathy A, et al. Among authors: jalvi r.
PLoS One. 2014 Jan 8;9(1):e84773. doi: 10.1371/journal.pone.0084773. eCollection 2014.
PLoS One. 2014.
PMID: 24416283
Free PMC article.
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Mutations in OTOF, CLDN14 & SLC26A4 genes as major causes of hearing impairment in Dhadkai village, Jammu & Kashmir, India.
Pandey N, Rashid T, Jalvi R, Sharma M, Rangasayee R, Andrabi KI, Anand A.
Pandey N, et al.
Indian J Med Res. 2017 Oct;146(4):489-497. doi: 10.4103/ijmr.IJMR_635_15.
Indian J Med Res. 2017.
PMID: 29434063
Free PMC article.
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Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India.
RamShankar M, Girirajan S, Dagan O, Ravi Shankar HM, Jalvi R, Rangasayee R, Avraham KB, Anand A.
RamShankar M, et al.
J Med Genet. 2003 May;40(5):e68. doi: 10.1136/jmg.40.5.e68.
J Med Genet. 2003.
PMID: 12746422
Free PMC article.
No abstract available.
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A novel locus DFNA59 for autosomal dominant nonsyndromic hearing loss maps at chromosome 11p14.2-q12.3.
Chatterjee A, Jalvi R, Pandey N, Rangasayee R, Anand A.
Chatterjee A, et al.
Hum Genet. 2009 Jan;124(6):669-75. doi: 10.1007/s00439-008-0596-3. Epub 2008 Nov 22.
Hum Genet. 2009.
PMID: 19030898
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