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Article

Single-nucleotide polymorphism arrays and unexpected consanguinity: considerations for clinicians when returning results to families.

Genetics in medicine : official journal of the American College of Medical Genetics - 1 May 2015

Delgado Fernanda, Tabor Holly K, Chow Penny M, Conta Jessie H, Feldman Kenneth W, Tsuchiya Karen D, Beck Anita E

Abstract excerpt

PURPOSE: The broad use of single-nucleotide polymorphism microarrays has increased identification of unexpected consanguinity. Therefore, guidelines to address reporting of consanguinity have been published for clinical laboratories. Because no such guidelines for clinicians exist, we describe a case and present recommendations for clinicians to disclose unexpected consanguinity to families. METHODS: In a boy...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 25232848
DOI: 10.1038/gim.2014.119
PMCID: PMC4404161

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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