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Article

Assignment of a locus for autosomal dominant idiopathic scoliosis (IS) to human chromosome 17p11.

Human genetics - 1 Oct 2002

Salehi Leila Baghernajad, Mangino Massimo, De Serio Salvatore, De Cicco Domenico, Capon Francesca, Semprini Sabrina, Pizzuti Antonio, Novelli Giuseppe, Dallapiccola Bruno

Abstract excerpt

Idiopathic scoliosis (IS) is a spine deformity of unknown etiology. Family studies have suggested that IS may be inherited as a mendelian autosomal dominant trait. We have performed linkage analysis on a three-generation IS Italian family. A positive LOD score value of 3.20 at theta=0.00 was detected with marker D17S799 after a genome-wide scanning. Analysis of six flanking microsatellites confirmed the linkage...

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Source

Identifiers

PMID: 12384783
DOI: 10.1007/s00439-002-0785-4

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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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