Preimplantation Genetic Diagnosis: Its Role in Prevention of Deafness
Author:
Publisher
Springer Science and Business Media LLC
Subject
Otorhinolaryngology,Surgery
Link
http://link.springer.com/content/pdf/10.1007/s12070-014-0711-9.pdf
Reference20 articles.
1. Taneja MK, Taneja Vivek (2012) Role of ENT Surgeon in National Deafness Program for Prevention and control of Deafness. Ind J Otol 18(3):119–121
2. del Castillo FJ, Rodriguez-Ballesteros M, Martin Y, Arellano B, Gallo-Teran J, Morales-Angulo C et al (2003) Heteroplasmy for the 1555A → G mutation in the mitochondrial 12s rRNA gene in six Spanish families with non-syndromic hearing loss. J Med Genet 40:632–636
3. Cryns K, Van Camp G (2004) Deafness genes and their diagnostic applications. Audiol Neurootol 9:2–22
4. Taneja MK (2012) Preimplantation genetic diagnosis and deafness. Indian J Otolaryngol Head Neck Surg 64(2):103–105
5. Baruch S (2005) Genetic testing of embryos: a critical need for data. Reprod Biomed Online 11:667
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1. Preimplantation genetic diagnosis of hereditary hearing loss: a narrative review;Journal of Bio-X Research;2021-08-19
2. Preimplantation Genetic Diagnosis in India: The Current Scenario and Potential Developments;Journal of Fetal Medicine;2018-02-22
3. Successful preimplantation genetic diagnosis by targeted next-generation sequencing on an ion torrent personal genome machine platform;Oncology Letters;2018-01-26
4. Deafness, a Social Stigma: Physician Perspective;Indian Journal of Otolaryngology and Head & Neck Surgery;2014-09-23
5. Screening and analysis of mutation hot-spots in deafness-associated genes among adolescents with hearing loss;Molecular Medicine Reports;2012-10-23
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