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Volumn 101, Issue 1, 2016, Pages 116-123

Post-mortem cytogenomic investigations in patients with congenital malformations

Author keywords

Congenital malformations; DNA copy number variations; Post mortem cytogenomic investigation

Indexed keywords

ARTICLE; AUTOPSY; CHROMOSOME ANALYSIS; CLINICAL ARTICLE; CONGENITAL HEART DISEASE; CONGENITAL MALFORMATION; CONTROLLED STUDY; COPY NUMBER VARIATION; CYTOGENETICS; DNA EXTRACTION; FLUORESCENCE IN SITU HYBRIDIZATION; GASTROINTESTINAL MALFORMATION; GENE DELETION; GENE DUPLICATION; GENE FREQUENCY; GENE IDENTIFICATION; GENETIC ASSOCIATION; GENETIC PROCEDURES; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; HUMAN; HUMAN TISSUE; JAW MALFORMATION; MICROSATELLITE MARKER; MISSENSE MUTATION; MOSAICISM; MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; NEUROLOGIC DISEASE; SANGER SEQUENCING; SHORT TANDEM REPEAT; SINGLE NUCLEOTIDE POLYMORPHISM; SKELETON MALFORMATION; TERATOLOGY; TISSUE DISTRIBUTION; UROGENITAL TRACT MALFORMATION; CONGENITAL DISORDER; GENETICS; HUMAN GENOME; MULTIPLEX POLYMERASE CHAIN REACTION; POSTMORTEM CHANGE; PROCEDURES; Y CHROMOSOME;

EID: 84979879959     PISSN: 00144800     EISSN: 10960945     Source Type: Journal    
DOI: 10.1016/j.yexmp.2016.07.003     Document Type: Article
Times cited : (4)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.