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Article

Male-to-male transmission in Laurin-Sandrow syndrome and exclusion of RARB and RARG.

American journal of medical genetics. Part A - 30 Aug 2005

Kjaer Klaus W, Hansen Lars, Eiberg Hans, Christensen Knud Stenild, Opitz John M, Tommerup Niels

Abstract excerpt

We report on a father and a son with nasal and limb defects characteristic of Laurin-Sandrow syndrome (LSS) excluding for the first time X-linked inheritance in this rare condition. Based on a search for genes expressed late during nose formation and early in limb formation we identified retinoic acid receptor B (RARB) and retinoic acid receptor G (RARG) as possible candidate genes and sequenced bidirectionally...

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

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Source

Identifiers

PMID: 16059937
DOI: 10.1002/ajmg.a.30820

Genes

RARB
RARG
LSS

Provenance

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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