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Volumn 9, Issue 6, 2014, Pages

X chromosome-linked CNVs in male infertility: Discovery of overall duplication load and recurrent, patient-specific gains with potential clinical relevance

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME ANALYSIS; CHROMOSOME DUPLICATION; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; COPY NUMBER VARIATION; DUP1A GENE; DUP20 GENE; DUP26 GENE; DUP40 GENE; DUP5 GENE; GENE; GENE CONTROL; GENE EXPRESSION; GENE FREQUENCY; GENE LOCUS; GENE MAPPING; GENETIC GAIN; GENETIC RECOMBINATION; GENETIC VARIABILITY; HUMAN; IDIOPATHIC DISEASE; MAJOR CLINICAL STUDY; MALE; MALE INFERTILITY; MEIOSIS; PAR1 GENE; PATHOGENESIS; POLYMERASE CHAIN REACTION; QUANTITATIVE ANALYSIS; SPERMATOGENESIS; TESTIS; TISSUE SPECIFICITY; X CHROMOSOME LINKAGE; CASE CONTROL STUDY; GENE DUPLICATION; GENETICS; X CHROMOSOME;

EID: 84902590088     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0097746     Document Type: Article
Times cited : (19)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.