Distinct breakpoints in two cases with deletion in the Yp11.2 region in Japanese population

Human Genetics

Volumn 127, Issue 5, 2010, Pages 537-543

  Kumagai, Reiko ^a   Sasaki, Yoshitoshi ^b   Tokuta, Takuya ^b   Biwasaka, Hitoshi ^b   Matsusue, Aya ^c   Aoki, Yasuhiro ^d   Dewa, Koji ^a  

^a IWATE MEDICAL UNIVERSITY   (Japan)

^b Iwate Prefecture Police Headquarters   (Japan)

^c FUKUOKA UNIVERSITY   (Japan)

^d NAGOYA CITY UNIVERSITY GRADUATE SCHOOL OF MEDICAL SCIENCES   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

AMELOGENIN; AMELY PROTEIN, HUMAN; PRIMER DNA;

ARTICLE; CASE REPORT; CHROMOSOME YP; ETHNIC GROUP; FORENSIC IDENTIFICATION; GENE DELETION; GENE LOCUS; GENE MAPPING; GENETIC MARKER; HAPLOTYPE; HOMOLOGOUS RECOMBINATION; HUMAN; JAPANESE; MALE; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; SEX DETERMINATION; ASIAN; DNA SEQUENCE; GENDER AND SEX; GENETICS; GENOTYPE; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; SINGLE NUCLEOTIDE POLYMORPHISM; Y CHROMOSOME;

AMELOGENIN; ASIAN CONTINENTAL ANCESTRY GROUP; BASE SEQUENCE; CHROMOSOMES, HUMAN, Y; DNA PRIMERS; GENETIC MARKERS; GENOTYPE; HAPLOTYPES; HUMANS; MALE; MOLECULAR SEQUENCE DATA; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE ANALYSIS, DNA; SEQUENCE DELETION; SEX DETERMINATION (GENETICS);

EID: 77951647957     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: 10.1007/s00439-010-0794-7     Document Type: Article

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