Nucleotide variation at Msn and Alas2, two genes flanking the centromere of the X chromosome in humans

Genetics

Volumn 167, Issue 1, 2004, Pages 423-437

  Nachman, Michael W ^a   D'Agostino, Susan L ^a   Tillquist, Christopher R ^b   Mobasher, Zahra ^b   Hammer, Michael F ^a,b  

^a University of Arizona   (United States)

^b UNIVERSITY OF ARIZONA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

5 AMINOLEVULINATE SYNTHASE; MOESIN;

ARTICLE; CENTROMERE; CLINICAL ARTICLE; DEMOGRAPHY; DNA FLANKING REGION; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENETIC DISTANCE; GENETIC RECOMBINATION; GENETIC SELECTION; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HUMAN; MALE; NONHUMAN; NORMAL HUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; X CHROMOSOME; X CHROMOSOME LINKAGE;

5-AMINOLEVULINATE SYNTHETASE; AFRICA; ANIMALS; CENTROMERE; HAPLOTYPES; HUMANS; LINKAGE (GENETICS); LINKAGE DISEQUILIBRIUM; MALE; MICROFILAMENT PROTEINS; MODELS, GENETIC; PAN TROGLODYTES; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; PONGO PYGMAEUS; RECOMBINATION, GENETIC; VARIATION (GENETICS); X CHROMOSOME;

PAN TROGLODYTES; PONGO PYGMAEUS;

EID: 2942624037     PISSN: 00166731     EISSN: None     Source Type: Journal    
DOI: 10.1534/genetics.167.1.423     Document Type: Article

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