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Volumn 271, Issue 1, 2005, Pages 19-21

Second-trimester genetic amniocentesis: 5-Yar experience

Author keywords

Amniocentesis; Anomaly screening; Prenatal diagnosis; Triple test; Ultrasonography

Indexed keywords

ADOLESCENT; ADULT; AMNIOCENTESIS; ARTICLE; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CONTROLLED STUDY; CORPUS CALLOSUM AGENESIS; DOWN SYNDROME; EVALUATION; EXPERIENCE; FEMALE; FETUS WASTAGE; GASTROSCHISIS; GENETIC SCREENING; HOSPITAL DEPARTMENT; HOSPITAL PERSONNEL; HUMAN; LITERATURE; MAJOR CLINICAL STUDY; MATERNAL AGE; MEDICAL RECORD; NEWBORN; OMPHALOCELE; PREGNANCY COMPLICATION; RELIABILITY; SAFETY; SECOND TRIMESTER PREGNANCY; SIBLING; ULTRASOUND; UNIVERSITY HOSPITAL;

EID: 12944302599     PISSN: 09320067     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00404-004-0635-9     Document Type: Article
Times cited : (14)

References (11)
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  • 2
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  • 3
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    • Estimating a woman's risk of having a pregnancy associated with Down's syndrome using her age and serum alpha-fetoprotein level
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    • (1987) Br J Obstet Gynaecol , vol.94 , pp. 387-402
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  • 4
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  • 7
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    • Contemporary approaches to prenatal diagnosis
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  • 8
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    • National Institute of Child Health and Human Development National Registry for Amniocentesis (NICHD) study group (1976) Midtrimester amniocentesis for prenatal diagnosis: safety and accuracy. J Am Med Assoc 236:1471-1476
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  • 10
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    • Serum screening for Down's syndrome between 8 and 14 weeks of pregnancy
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    • Wald, N.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.