Utility of clinical exome sequencing in the evaluation of neonates with suspected genetic condition – An observational study from tertiary neonatal care unit in South India

To study the utility of clinical exome sequencing (CES) using next generation sequencing (NGS) in evaluating neonates with suspected genetic conditions. This is an observational study conducted in a tertiary care neonatal unit. We included neonates with suspected genetic conditions, for whom CES wer...

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Veröffentlicht in:	European journal of medical genetics 2021-07, Vol.64 (7), p.104247-104247, Article 104247
Hauptverfasser:	Usha Devi, R., Thinesh Kumar, J., Jan, Shaik Mohammad Shafi, Chandrasekaran, Ashok, Amboiram, Prakash, Koshy, Teena, Balakrishnan, Umamaheswari
Format:	Artikel
Sprache:	eng
Schlagworte:	Disorders Exome sequencing Genetics Heterogeneity Variants
Online-Zugang:	Volltext
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