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PMID: 2565870 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

A new polymorphic marker very closely linked to DXS52 in the q28 region of the human X chromosome.

Human genetics ·Vol. 82 ·No. 1 ·1989-04-00 ·Pages 85-6

Vincent A, Kretz C, Oberlé I, Mandel JL

Abstract

We have isolated an X chromosome probe, St35.691 (DXS305), which detects two RFLPs with TaqI and PstI, whose combined heterozygosity is about 60%. This probe has been assigned to Xq28 by physical and genetic mapping and is very closely linked to DXS52, DXS15, and the coagulation factor VIII gene (F8C). The best estimate of the recombination fraction for the DXS52-DXS305 interval is 0.014, with a lod score of 50.1. Multipoint analysis places DXS305 on the same side of F8C as DXS52, but complete ordering of the three loci was not possible with our present data. This highly informative marker should be useful in the precise mapping of the many disease genes that have been assigned to the Xq28 band.

MeSH Terms
DNA Probes Genetic Linkage Humans Polymorphism, Genetic Polymorphism, Restriction Fragment Length Recombination, Genetic X Chromosome/ultrastructure
Chemicals
DNA Probes
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Vincent A
Laboratoire de Génétique Moléculaire des Eucaryotes du CNRS, Unité 184 de Biologie Moléculaire et de Génie Génétique de l'INSERM, Faculté de Médecine, Strasbourg, France.
Kretz C
Oberlé I
Mandel J L
References (8)
8 references, click to expand
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Article Info
Journal
Human genetics
Abbr.
Hum Genet
ISSN
0340-6717
Published
1989-04-00
Pages
85-6
Language
English
Region
Germany
NLM ID
7613873
Subset
IM
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