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Article

Carrier screening for single gene disorders.

Seminars in fetal & neonatal medicine - 1 Apr 2018

Rose Nancy C, Wick Myra

Abstract excerpt

Screening for genetic disorders began in 1963 with the initiation of newborn screening for phenylketonuria. Advances in molecular technology have made both newborn screening for newborns affected with serious disorders, and carrier screening of individuals at risk for offspring with genetic disorders, more complex and more widely available. Carrier screening today can be performed secondary to family...

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Identifiers

PMID: 28669541
DOI: 10.1016/j.siny.2017.06.001

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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