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Volumn 8, Issue 6, 2015, Pages 682-689

Transcriptional Impact of Rare and Private Copy Number Variants in Hypoplastic Left Heart Syndrome

Author keywords

Cardiovascular diseases; Congenital; Genetics; Heart defects

Indexed keywords

3' UNTRANSLATED REGION; ADULT; ARTICLE; CONTROLLED STUDY; COPY NUMBER VARIATION; FETUS; GENE AMPLIFICATION; GENE DELETION; GENE EXPRESSION REGULATION; GENE FREQUENCY; GENE IDENTIFICATION; GENETIC ASSOCIATION; HETEROZYGOSITY; HUMAN; HYPOPLASTIC LEFT HEART SYNDROME; MAJOR CLINICAL STUDY; PATHOGENESIS; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; UPREGULATION; ANIMAL; COHORT ANALYSIS; CONGENITAL HEART MALFORMATION; DNA MICROARRAY; EXON; FEMALE; GENETIC TRANSCRIPTION; GENETICS; GENOTYPE; MALE; MARKOV CHAIN; METABOLISM; MOUSE; PHENOTYPE; POLYMERASE CHAIN REACTION;

EID: 84952988675     PISSN: 17528054     EISSN: 17528062     Source Type: Journal    
DOI: 10.1111/cts.12340     Document Type: Article
Times cited : (12)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.