Document Detail


Tetranucleotide short tandem repeat polymorphisms and their possible mode of origin.
MedLine Citation:
PMID:  9678331     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
An analysis of three autosomal, one X-chromosomal, and one Y-chromosomal tetranucleotide short tandem repeat loci in a large southern German population sample (including family studies) and in several nonhuman primate species revealed remarkable similarities in structure of already known and some newly detected alleles and in allele frequency distributions. These similarities, which are briefly discussed, can best be explained by transspecific evolution, followed by gene-conversion-like mutational events.
Authors:
K Bender; G Beller; S Lautsch
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Cytogenetics and cell genetics     Volume:  80     ISSN:  0301-0171     ISO Abbreviation:  Cytogenet. Cell Genet.     Publication Date:  1998  
Date Detail:
Created Date:  1998-08-21     Completed Date:  1998-08-21     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0367735     Medline TA:  Cytogenet Cell Genet     Country:  SWITZERLAND    
Other Details:
Languages:  eng     Pagination:  34-6     Citation Subset:  IM    
Affiliation:
Institut für Humangenetik und Anthropologie der Universität Freiburg, Germany.
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MeSH Terms
Descriptor/Qualifier:
Alleles
Animals
Callitrichinae / genetics
Cebidae / genetics
Child
Evolution, Molecular*
Fibrinogen / genetics
Gene Frequency
Hominidae / genetics
Humans
Microsatellite Repeats*
Polymorphism, Genetic*
Chemical
Reg. No./Substance:
9001-32-5/Fibrinogen

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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