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Article

Splotch locus mouse mutants: models for neural tube defects and Waardenburg syndrome type I in humans.

Journal of medical genetics - 1 Mar 1992

Moase C E, Trasler D G

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 1552554
DOI: 10.1136/jmg.29.3.145
PMCID: PMC1015886

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Splotch locus mouse mutants: models for neural tube defects and Waardenburg syndrome type I in humans.PMID 1552554Read ↗

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Mouse models for understanding human developmental anomalies.Semantic proximity Read ↗

Waardenburg syndrome in man and splotch mutants in the mouse: a paradigm of the usefulness of linkage and synteny homologies in mouse and man for the genetic analysis of human congenital malformations.Semantic proximity Read ↗

NEW SPLOTCH ALLELES IN THE MOUSE.Semantic proximity Read ↗

An update to the list of mouse mutants with neural tube closure defects and advances toward a complete genetic perspective of neural tube closure.Semantic proximity Read ↗

Normal hearing in Splotch (Sp/+), the mouse homologue of Waardenburg syndrome type 1.Semantic proximity Read ↗

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