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Volumn 4, Issue 3, 2010, Pages 271-274

Current situation and development of prenatal diagnosis in China

Author keywords

China; prenatal diagnosis; prenatal screening

Indexed keywords

AMNIOCENTESIS; CHINA; CHROMOSOME ABERRATION; CONGENITAL DISORDER; ETHICS; FEMALE; FETUS DISEASE; FETUS ECHOGRAPHY; GENETIC DISORDER; HUMAN; PREGNANCY; PRENATAL DEVELOPMENT; PRENATAL DIAGNOSIS; REVIEW; STATISTICS;

EID: 77956648727     PISSN: 16737342     EISSN: 16737458     Source Type: Journal    
DOI: 10.1007/s11684-010-0100-z     Document Type: Review
Times cited : (10)

References (9)
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    • First-trimester ADAM12 and PAPP-A as markers for intrauterine fetal growth restriction through their roles in the insulin-like growth factor system
    • Cowans N J, Spencer K. First-trimester ADAM12 and PAPP-A as markers for intrauterine fetal growth restriction through their roles in the insulin-like growth factor system. Prenat Diagn, 2007, 27(3): 264-271.
    • (2007) Prenat Diagn , vol.27 , Issue.3 , pp. 264-271
    • Cowans, N.J.1    Spencer, K.2
  • 5
    • 0036140193 scopus 로고    scopus 로고
    • Differential DNA methylation between fetus and mother as a strategy for detecting fetal DNA in maternal plasma
    • Poon L L, Leung T N, Lau T K, Chow K C, Lo Y M D. Differential DNA methylation between fetus and mother as a strategy for detecting fetal DNA in maternal plasma. Clin Chem, 2002, 48(1): 35-41.
    • (2002) Clin Chem , vol.48 , Issue.1 , pp. 35-41
    • Poon, L.L.1    Leung, T.N.2    Lau, T.K.3    Chow, K.C.4    Lo, Y.M.D.5
  • 6
    • 44449141793 scopus 로고    scopus 로고
    • Development and evaluation of a reverse dot blot assay for the simultaneous detection of six common Chinese G6PD mutations and one polymorphism
    • Li L, Zhou Y Q, Xiao Q Z, Yan T Z, Xu X M. Development and evaluation of a reverse dot blot assay for the simultaneous detection of six common Chinese G6PD mutations and one polymorphism. Blood Cells Mol Dis, 2008, 41(1): 17-21.
    • (2008) Blood Cells Mol Dis , vol.41 , Issue.1 , pp. 17-21
    • Li, L.1    Zhou, Y.Q.2    Xiao, Q.Z.3    Yan, T.Z.4    Xu, X.M.5
  • 7
    • 44449130819 scopus 로고    scopus 로고
    • Identification of a novel frameshift mutation at codon 53 (-T) in the beta-globin gene causing dominantly inherited beta-thalassemia in a Chinese Miao family
    • Yi P, Yu F, Huang S, Zhong C, Li Q, Yang Y, Zhang W, Xiao C, Xu X. Identification of a novel frameshift mutation at codon 53 (-T) in the beta-globin gene causing dominantly inherited beta-thalassemia in a Chinese Miao family. Blood Cells Mol Dis, 2008, 41(1): 56-59.
    • (2008) Blood Cells Mol Dis , vol.41 , Issue.1 , pp. 56-59
    • Yi, P.1    Yu, F.2    Huang, S.3    Zhong, C.4    Li, Q.5    Yang, Y.6    Zhang, W.7    Xiao, C.8    Xu, X.9
  • 9
    • 76449088558 scopus 로고    scopus 로고
    • Contribution of MRI to detect further anomalies in fetal ventriculomegaly
    • Yin S, Na Q, Chen J, Li-Ling J, Liu C. Contribution of MRI to detect further anomalies in fetal ventriculomegaly. Fetal Diagn Ther, 2010, 27(1): 20-24.
    • (2010) Fetal Diagn Ther , vol.27 , Issue.1 , pp. 20-24
    • Yin, S.1    Na, Q.2    Chen, J.3    Li-Ling, J.4    Liu, C.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.