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Article

Common polymorphism in H19 associated with birthweight and cord blood IGF-II levels in humans.

BMC genetics - 10 May 2005

Petry Clive J, Ong Ken K, Barratt Bryan J, Wingate Diane, Cordell Heather J, Ring Susan M, Pembrey Marcus E, Reik Wolf, Todd John A, Dunger David B

Abstract excerpt

BACKGROUND: Common genetic variation at genes that are imprinted and exclusively maternally expressed could explain the apparent maternal-specific inheritance of low birthweight reported in large family pedigrees. We identified ten single nucleotide polymorphisms (SNPs) in H19, and we genotyped three of these SNPs in families from the contemporary ALSPAC UK birth cohort (1,696 children, 822 mothers and 661...

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Identifiers

PMID: 15885138
DOI: 10.1186/1471-2156-6-22
PMCID: PMC1140752

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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