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Page 1
PNPT1, MYO15A, PTPRQ, and SLC12A2-associated genetic and phenotypic heterogeneity among hearing impaired assortative mating families in Southern India.
Ann Hum Genet. 2022 Jan;86(1):1-13. doi: 10.1111/ahg.12442. Epub 2021 Aug 9.
Ann Hum Genet. 2022.
PMID: 34374074
Low incidence of GIPC3 variants among the prelingual hearing impaired from southern India.
Kalaimathi M, Subathra M, Jeffrey JM, Selvakumari M, Chandru J, Sharanya N, Paridhy VS, Srisailapathy CRS.
Kalaimathi M, et al. Among authors: chandru j.
J Genet. 2020;99:74.
J Genet. 2020.
PMID: 33168789
Free article.
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Genetic analysis of SLC26A4 gene (pendrin) related deafness among a cohort of assortative mating families from southern India.
Chandru J, Jeffrey JM, Pavithra A, Vanniya SP, Devi GN, Mahalingam S, Karthikeyen NP, Srisailapathy CRS.
Chandru J, et al.
Eur Arch Otorhinolaryngol. 2020 Nov;277(11):3021-3035. doi: 10.1007/s00405-020-06026-3. Epub 2020 May 16.
Eur Arch Otorhinolaryngol. 2020.
PMID: 32417962
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Role of DFNB1 mutations in hereditary hearing loss among assortative mating hearing impaired families from South India.
Amritkumar P, Jeffrey JM, Chandru J, Vanniya S P, Kalaimathi M, Ramakrishnan R, Karthikeyen NP, Srikumari Srisailapathy CR.
Amritkumar P, et al. Among authors: chandru j.
BMC Med Genet. 2018 Jun 19;19(1):105. doi: 10.1186/s12881-018-0609-6.
BMC Med Genet. 2018.
PMID: 29921236
Free PMC article.
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Recurrence of reported CDH23 mutations causing DFNB12 in a special cohort of South Indian hearing impaired assortative mating families - an evaluation.
Vanniya S P, Chandru J, Pavithra A, Jeffrey JM, Kalaimathi M, Ramakrishnan R, Karthikeyen NP, C R Srikumari S.
Vanniya S P, et al. Among authors: chandru j.
Ann Hum Genet. 2018 Mar;82(2):119-126. doi: 10.1111/ahg.12228. Epub 2017 Nov 17.
Ann Hum Genet. 2018.
PMID: 29148562
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High incidence of GJB2 gene mutations among assortatively mating hearing impaired families in Kerala: future implications.
Pavithra A, Jeffrey JM, Chandru J, Ramesh A, Srisailapathy CR.
Pavithra A, et al. Among authors: chandru j.
J Genet. 2014 Apr;93(1):207-13. doi: 10.1007/s12041-014-0338-3.
J Genet. 2014.
PMID: 24840842
Free article.
No abstract available.
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Rare compound heterozygosity involving dominant and recessive mutations of GJB2 gene in an assortative mating hearing impaired Indian family.
Pavithra A, Chandru J, Jeffrey JM, Karthikeyen NP, Srisailapathy CRS.
Pavithra A, et al. Among authors: chandru j.
Eur Arch Otorhinolaryngol. 2017 Jan;274(1):119-125. doi: 10.1007/s00405-016-4229-5. Epub 2016 Aug 1.
Eur Arch Otorhinolaryngol. 2017.
PMID: 27481527
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