Document Detail


Inheritance of some electrophoretic phenotypes of human hair.
MedLine Citation:
PMID:  1697558     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Four isokeratin patterns were demonstrated by means of one-dimensional SDS electrophoresis of low sulfur proteins in human hair. The phenotypes had the following frequencies: K1 = 69.70%, K1m = 18.18%, K3 = 9.09%, K3m = 3.03%. Pedigree analysis and evaluation of observed and expected frequencies of the phenotypes gave rise to the conclusion that the phenotypes are controlled by genes of two independent autosomal loci K and m. We believe that *K3 and *m are dominant, whereas *K1 and *non-m are recessive.
Authors:
M Schimkat; M P Baur; J Henke
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Human genetics     Volume:  85     ISSN:  0340-6717     ISO Abbreviation:  Hum. Genet.     Publication Date:  1990 Aug 
Date Detail:
Created Date:  1990-10-10     Completed Date:  1990-10-10     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  7613873     Medline TA:  Hum Genet     Country:  GERMANY, WEST    
Other Details:
Languages:  eng     Pagination:  311-4     Citation Subset:  IM    
Affiliation:
Laboratorium für forensische Blutgruppenkunde, Düsseldorf, Federal Republic of Germany.
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MeSH Terms
Descriptor/Qualifier:
Electrophoresis, Polyacrylamide Gel
Female
Hair / analysis*
Humans
Keratins / analysis,  genetics*
Male
Pedigree
Phenotype
Chemical
Reg. No./Substance:
68238-35-7/Keratins

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


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