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Article

Autozygosity mapping of a seckel syndrome locus to chromosome 3q22. 1-q24.

American journal of human genetics - 1 Aug 2000

Goodship J, Gill H, Carter J, Jackson A, Splitt M, Wright M

Abstract excerpt

Seckel syndrome (MIM 210600) is an autosomal recessive disorder of low birth weight, severe microcephaly, and dysmorphic facial appearance with receding forehead, prominent nose, and micrognathia. We have performed a genomic screen in two consanguineous families of Pakistani origin and found that the disorder segregates with markers between loci D3S1316 and D3S3710, which map to chromosome 3q22.1-q24. Analysis...

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Identifiers

PMID: 10889046
DOI: 10.1086/303023
PMCID: PMC1287195

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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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