Evaluating the Utility of Next Generation Sequencing Technology in the Diagnosis and Prevention of Genetic Disorders in India, the Early Experiences
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s40556-019-00204-y.pdf
Reference25 articles.
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3. Nampoothiri S, Yeshodharan D, Sainulabdin G, Narayanan D, Padmanabhan L, Girisha KM, et al. Eight years experience from a skeletal dysplasia referral center in a tertiary Hospital in Southern India. A model for the diagnosis and treatment of rare diseases in a developing country. Am J Med Genet A. 2014;164(A(9)):2317–23.
4. Balarajan Y, Selvaraj S, Subramnaian SV. Health care and equity in India. The Lancet. 2011;337(9764):505–15.
5. Nahar R, Puri RD, Saxena R, Verma IC. Do parental perceptions and motivations towards genetic testing and prenatal diagnosis for deafness vary in different cultures. Am J Med Genet A. 2013;161A(1):76–81.
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