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.

Gespeichert in:
Autor*in:

Usha Devi, R. [verfasserIn]

Thinesh Kumar, J.

Jan, Shaik Mohammad Shafi

Chandrasekaran, Ashok

Amboiram, Prakash

Koshy, Teena

Balakrishnan, Umamaheswari

Format:

E-Artikel

Sprache:

Englisch

Erschienen:

2021

Schlagwörter:

Heterogeneity

Variants

Exome sequencing

Disorders

Genetics

Übergeordnetes Werk:

Enthalten in: Edge minimization in de Bruijn graphs - Baier, Uwe ELSEVIER, 2021, New York, NY [u.a.]

Übergeordnetes Werk:

volume:64 ; year:2021 ; number:7 ; pages:0

Links:

Volltext

DOI / URN:

10.1016/j.ejmg.2021.104247

Katalog-ID:

ELV054427371

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