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Volumn 3, Issue 4, 2009, Pages 265-267
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A rare mutation in the primer binding region of the Amelogenin X homologue gene
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Author keywords
Amelogenin gene; Polish population; X homologue null allele
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Indexed keywords
AMELOGENIN;
AMINO ACID SUBSTITUTION;
AMPLICON;
ANALYTICAL EQUIPMENT;
ARTICLE;
CONTROLLED STUDY;
DNA SEQUENCE;
FORENSIC GENETICS;
GENE AMPLIFICATION;
GENE LOCUS;
GENE MUTATION;
GENOTYPE;
HUMAN;
MALE;
MUTATIONAL ANALYSIS;
NUCLEOTIDE SEQUENCE;
POLAND;
PRIORITY JOURNAL;
SEQUENCE ANALYSIS;
SHORT TANDEM REPEAT;
X CHROMOSOME;
ALLELES;
AMELOGENIN;
CASE-CONTROL STUDIES;
CHROMOSOMES, HUMAN, X;
DNA;
DNA PRIMERS;
EUROPEAN CONTINENTAL ANCESTRY GROUP;
FORENSIC GENETICS;
GENETICS, POPULATION;
HUMANS;
MALE;
MUTATION;
NUCLEIC ACID AMPLIFICATION TECHNIQUES;
POLAND;
POPULATION GROUPS;
REFERENCE STANDARDS;
SEQUENCE ANALYSIS, DNA;
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EID: 67651244054
PISSN: 18724973
EISSN: None
Source Type: Journal
DOI: 10.1016/j.fsigen.2009.01.010 Document Type: Article |
Times cited : (27)
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References (11)
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