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Volumn 25, Issue SUPPL. 1, 2012, Pages 25-29

Congenital malformations

Author keywords

Association; Blastogenesis; Chromosome; Counseling; Gene; Imprinting; Methylation; Phenotype; Sequence; Syndrome; Uniparental dysomy

Indexed keywords

CHONDRODYSPLASIA; CHROMOSOME ABERRATION; CONFERENCE PAPER; CONGENITAL HEART DISEASE; CONGENITAL MALFORMATION; CRANIOFACIAL MALFORMATION; DISEASE CLASSIFICATION; DISEASE COURSE; DISEASE SEVERITY; DOWN SYNDROME; DYSOSTOSIS; EDWARDS SYNDROME; ENVIRONMENTAL FACTOR; FAMILIAL DISEASE; GENETIC ASSOCIATION; GENETIC COUNSELING; GENETIC SCREENING; HEREDITY; HUMAN; LIFE EXPECTANCY; MORBIDITY; MORTALITY; PATAU SYNDROME; PATHOPHYSIOLOGY; PHENOTYPE; PRENATAL DEVELOPMENT; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; PUBLIC HEALTH SERVICE; RECURRENCE RISK; RISK ASSESSMENT; RISK FACTOR;

EID: 84859381926     PISSN: 14767058     EISSN: 14764954     Source Type: Journal    
DOI: 10.3109/14767058.2012.664943     Document Type: Review
Times cited : (103)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.