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PMID: 2985491 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X site.

Human genetics ·Vol. 69 ·No. 4 ·1985-00-00 ·Pages 327-31

Mattei MG, Baeteman MA, Heilig R, Oberlé I, Davies K, Mandel JL, Mattei JF

Abstract

The coagulation factor IX gene and two other polymorphic loci corresponding to DNA probes 52 A and St 14 have been previously localized in the q27 to qter region of the human X chromosome. In order to study their localization with respect to the fragile site at Xq27-28, we have hybridized the three DNA probes to metaphase chromosomes of a boy with fragile X mental retardation. We show that probe 52 A is located in the proximal part of the Xq27 band, while the coagulation factor IX gene is on the distal part of this band, but proximal to the fragile site. The very polymorphic St 14 probe is located in the distal part of the Xq28 band, on the other side of the fragile site.

MeSH Terms
Chromosome Banding Chromosome Fragile Sites Chromosome Fragility Chromosome Mapping DNA/genetics DNA Restriction Enzymes Factor IX/genetics Female Genetic Markers Humans Karyotyping Nucleic Acid Hybridization Polymorphism, Genetic X Chromosome
Chemicals
Genetic Markers Factor IX DNA DNA Restriction Enzymes
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Mattei M G
Baeteman M A
Heilig R
Oberlé I
Davies K
Mandel J L
Mattei J F
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17 references, click to expand
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Article Info
Journal
Human genetics
Abbr.
Hum Genet
ISSN
0340-6717
Published
1985-00-00
Pages
327-31
Language
English
Region
Germany
NLM ID
7613873
Subset
IM
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