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Volumn 81, Issue 2, 2017, Pages 282-285

An opportunity to address the genetic causes of birth defects

Author keywords

[No Author keywords available]

Indexed keywords

CHILDHOOD CANCER; COMPREHENSION; CONGENITAL MALFORMATION; COST; DISEASE ASSOCIATION; GENETIC ANALYSIS; GENETICS; HUMAN; MEDICAL RESEARCH; NONHUMAN; NOTE; PHENOTYPE; PRIORITY JOURNAL; PUBLIC HEALTH; SOCIETY; ANIMAL; CONGENITAL DISORDER; GENETIC PREDISPOSITION; NEWBORN; PATIENT CARE;

EID: 85012934011     PISSN: 00313998     EISSN: 15300447     Source Type: Journal    
DOI: 10.1038/pr.2016.229     Document Type: Note
Times cited : (13)

References (14)
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  • 5
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    • Estimates of the economic costs of birth defects
    • Waitzman NJ, Romano PS, Schefer RM. Estimates of the economic costs of birth defects. Inquiry 1994;31:188-205.
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    • Waitzman, N.J.1    Romano, P.S.2    Schefer, R.M.3
  • 7
    • 79951551816 scopus 로고    scopus 로고
    • United States Department of Health and Human Services Table 10
    • United States Department of Health and Human Services. Deaths: Final Data for 2013. (Table 10). (http://www.cdc.gov/nchs/data/nvsr/nvsr64/ nvsr64-02.pdf).
    • Deaths: Final Data for 2013
  • 9
    • 84880420496 scopus 로고    scopus 로고
    • Cancer risk in children and adolescents with birth defects: A population-based cohort study
    • Botto LD, Flood T, Little J, et al. Cancer risk in children and adolescents with birth defects: a population-based cohort study. PLoS One 2013;8: e69077.
    • (2013) PLoS One , vol.8 , pp. e69077
    • Botto, L.D.1    Flood, T.2    Little, J.3
  • 10
    • 84862492680 scopus 로고    scopus 로고
    • Are children with birth defects at higher risk of childhood cancers?
    • Carozza SE, Langlois PH, Miller EA, Canfeld M. Are children with birth defects at higher risk of childhood cancers? Am J Epidemiol 2012;175:1217-24.
    • (2012) Am J Epidemiol , vol.175 , pp. 1217-1224
    • Carozza, S.E.1    Langlois, P.H.2    Miller, E.A.3    Canfeld, M.4
  • 11
    • 84874248574 scopus 로고    scopus 로고
    • The Congenital Heart Disease Genetic Network Study: Rationale, design, and early results
    • Pediatric Cardiac Genomics Consortium
    • Gelb B, Brueckner M, Chung W, et al.; Pediatric Cardiac Genomics Consortium. The Congenital Heart Disease Genetic Network Study: rationale, design, and early results. Circ Res 2013;112:698-706.
    • (2013) Circ Res , vol.112 , pp. 698-706
    • Gelb, B.1    Brueckner, M.2    Chung, W.3
  • 12
    • 79952584346 scopus 로고    scopus 로고
    • Rare copy number variations in congenital heart disease patients identify unique genes in lef-right patterning
    • Fakhro KA, Choi M, Ware SM, et al. Rare copy number variations in congenital heart disease patients identify unique genes in lef-right patterning. Proc Natl Acad Sci USA 2011;108:2915-20.
    • (2011) Proc Natl Acad Sci USA , vol.108 , pp. 2915-2920
    • Fakhro, K.A.1    Choi, M.2    Ware, S.M.3
  • 13
    • 84927786478 scopus 로고    scopus 로고
    • Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data
    • Glessner JT, Bick AG, Ito K, et al. Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data. Circ Res 2014;115:884-96.
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    • Glessner, J.T.1    Bick, A.G.2    Ito, K.3
  • 14
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    • De novo mutations in histone-modifying genes in congenital heart disease
    • Zaidi S, Choi M, Wakimoto H, et al. De novo mutations in histone-modifying genes in congenital heart disease. Nature 2013;498:220-3.
    • (2013) Nature , vol.498 , pp. 220-223
    • Zaidi, S.1    Choi, M.2    Wakimoto, H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.