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Article

Fish mapping of a translocation breakpoint at 6q21 (or q22) in a patient with heterotaxia.

The Japanese journal of human genetics - 1 Dec 1997

Kato R, Matsumoto N, Fujimoto M, Nakano M, Nakamura Y, Niikawa N

Abstract excerpt

Heterotaxia is a congenital lateralization defect of visceral organs. As several single-genes that act on the formation of left-right asymmetry during embryogenesis have been identified in animals, a defect in the similar system may play a role in heterotaxia in man. We previously reported a Japanese girl with heterotaxia associated with a de novo balanced translocation (6;18)(q21 or q22;q21.3 or q22). In the...

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

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Source

Identifiers

PMID: 9560952
DOI: 10.1007/BF02767029

Genes

STS

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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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