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Article

Genomic organisation of the human chordin gene and mutation screening of candidate Cornelia de Lange syndrome genes.

Human genetics - 1 Jan 2000

Smith M, Herrell S, Lusher M, Lako L, Simpson C, Wiestner A, Skoda R, Ireland M, Strachan T

Abstract excerpt

We have determined the genomic organisation of the human chordin gene, CHRD, and have shown that it maps within a gene cluster at 3q27 containing THPO (thrombopoietin), CLCN2 (a voltage-gated chloride-channel gene) and EIF4G1 (a eukaryotic translation-initiation-factor-gamma gene). The CHRD and T...

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Source

Identifiers

PMID: 10480362
DOI: 10.1007/s004399900068

Genes

CHRD
GSC
SOX2
THPO
CLCN2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-10480362-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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