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PMID: 1685139 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Physical mapping of 60 DNA markers in the p21.1----q21.3 region of the human X chromosome.

Genomics ·Vol. 11 ·No. 2 ·1991-10-00 ·Pages 352-63

Lafrenière RG, Brown CJ, Powers VE, Carrel L, Davies KE, Barker DF, Willard HF

Abstract

Using a panel of human/rodent somatic cell hybrids and human lymphoblast lines segregating 18 different human X-chromosome rearrangements and deletions, we have assigned 60 DNA markers to the physical map of the X chromosome from Xp21.1 to Xq21.3. Data from Southern blot hybridization and polymerase chain reaction (PCR) amplification assign these markers to 15 primary map intervals. This provides a basis for further long-range cloning and mapping of the pericentromeric region of the X chromosome.

MeSH Terms
Base Sequence Cell Line Centromere Chromosome Aberrations/genetics Chromosome Mapping Chromosomes, Human DNA Probes Genetic Markers Humans Hybrid Cells Molecular Sequence Data Polymerase Chain Reaction Polymorphism, Restriction Fragment Length Tumor Cells, Cultured X Chromosome
Chemicals
DNA Probes Genetic Markers
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Lafrenière R G
Department of Genetics, Stanford University School of Medicine, California 94305.
Brown C J
Powers V E
Carrel L
Davies K E
Barker D F
Willard H F
Article Info
Journal
Genomics
Abbr.
Genomics
ISSN
0888-7543
Published
1991-10-00
Pages
352-63
Language
English
Region
United States
NLM ID
8800135
Subset
IM
Grants
NHGRI NIH HHS · HG00013 · United States
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