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Localization of the human gene for fibulin-1 (FBLN1) to chromosome band 22q13.3.

作者信息

Korenberg J R, Chen X N, Tran H, Argraves W S

机构信息

Medical Genetics-Birth Defects Center, Cedars-Sinai Medical Center, Los Angeles, CA.

出版信息

Cytogenet Cell Genet. 1995;68(3-4):192-3. doi: 10.1159/000133911.

DOI:10.1159/000133911
PMID:7842734
Abstract

Using fibulin-1 cDNA probes, we performed fluorescence in situ hybridization to map the human chromosomal location of the gene encoding the extracellular matrix and blood glycoprotein, fibulin-1 (FBLN1). The gene for fibulin-1 was mapped to a single site on the long arm of human chromosome 22 (22q13.3). The assignment of the chromosomal map position for the fibulin-1 gene will aid in the evaluation of its potential roles in human connective tissue and blood diseases.

摘要

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3
The fibulin-1 gene (FBLN1) is disrupted in a t(12;22) associated with a complex type of synpolydactyly.
在与一种复杂类型的并指多指畸形相关的t(12;22)中,纤维连接蛋白-1基因(FBLN1)被破坏。
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