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Article

Localization of a gene for syndactyly type 1 to chromosome 2q34-q36.

American journal of human genetics - 1 Aug 2000

Bosse K, Betz R C, Lee Y A, Wienker T F, Reis A, Kleen H, Propping P, Cichon S, Nöthen M M

Abstract excerpt

Syndactyly type 1 (SD1) is an autosomal dominant limb malformation characterized in its classical form by complete or partial webbing between the third and fourth fingers and/or the second and third toes. After exclusion of a candidate region previously identified for syndactyly type 2 (synpolydactyly), we performed a genomewide linkage analysis in a large German pedigree. We found evidence for linkage of SD1 to...

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Identifiers

PMID: 10877983
DOI: 10.1086/303028
PMCID: PMC1287194

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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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