» Articles » PMID: 9024576

European Gene Mapping Project (EUROGEM): Breakpoint Panels for Human Chromosomes Based on the CEPH Reference Families. Centre D'Etude Du Polymorphisme Humain

Abstract

Meiotic breakpoint panels for human chromosomes 2, 3, 4, 5, 6, 7, 8, 9, 10, 13, 14, 15, 17, 18, 20 and X were constructed from genotypes from the CEPH reference families. Each recombinant chromosome included has a breakpoint well-supported with reference to defined quantitative criteria. The panels were constructed at both a low-resolution, useful for a first-pass localization, and high-resolution, for a more precise placement. The availability of such panels will reduce the number of genotyping experiments necessary to order new polymorphisms with respect to existing genetic markers. This paper shows only a representative sample of the breakpoints detected. The complete data are available on the World Wide Web (URL http:/(/)www.icnet.uk/axp/hgr/eurogem++ +/HTML/data.html) or by anonymous ftp (ftp.gene.ucl.ac.uk in/pub/eurogem/maps/breakpoints).

Citing Articles

DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss.

Hildebrand M, Morin M, Meyer N, Mayo F, Modamio-Hoybjor S, Mencia A Hum Mutat. 2011; 32(7):825-34.

PMID: 21520338 PMC: 3326665. DOI: 10.1002/humu.21512.