메뉴 건너뛰기




Volumn 15, Issue 1, 2004, Pages 53-59

Trends in cytogenetic prenatal diagnosis in a reference hospital in Izmir/Turkey: A comperative study for four years

Author keywords

Amniocentesis; Prenatal diagnosis; Trends

Indexed keywords

ADULT; AMNIOCENTESIS; ARTICLE; CHORION VILLUS SAMPLING; CHROMOSOME ANALYSIS; CHROMOSOME DISORDER; COMPARATIVE STUDY; CYTOGENETICS; EXPERIENCE; FEMALE; FETUS BLOOD SAMPLING; FETUS MALFORMATION; HUMAN; KARYOTYPE; MAJOR CLINICAL STUDY; MALE; PRENATAL DIAGNOSIS; SECOND TRIMESTER PREGNANCY; TURKEY (REPUBLIC);

EID: 12144289745     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (4)

References (24)
  • 1
    • 0032517538 scopus 로고    scopus 로고
    • 6-Year experience of prenatal diagnosis in an unselected population in Oxford, UK
    • BOYD P. A., CHAMBERLAIN P, HICKS N.R.: 6-year experience of prenatal diagnosis in an unselected population in Oxford, UK. Lancet, 1998, 352, 1577-1581.
    • (1998) Lancet , vol.352 , pp. 1577-1581
    • Boyd, P.A.1    Chamberlain, P.2    Hicks, N.R.3
  • 2
    • 0033555450 scopus 로고    scopus 로고
    • Frequencies of chromosomal abnormalities at amniocentesis: Over 20 years of cytogenetic analyses in one laboratory
    • CARON L., TIHY F, DALLAIRE L.: Frequencies of chromosomal abnormalities at amniocentesis: over 20 years of cytogenetic analyses in one laboratory. Am. J. Med. Genet., 1999, 82, 149-154.
    • (1999) Am. J. Med. Genet. , vol.82 , pp. 149-154
    • Caron, L.1    Tihy, F.2    Dallaire, L.3
  • 4
    • 1642471074 scopus 로고    scopus 로고
    • Evaluation of 437 amniotic fluid samples in prenatal diagnosis
    • COGULU O., TAS M.A., BOZOKLAR R., OZKINAY F.: Evaluation of 437 amniotic fluid samples in prenatal diagnosis. J. Neonatology. 1998, 5, 25-29.
    • (1998) J. Neonatology , vol.5 , pp. 25-29
    • Cogulu, O.1    Tas, M.A.2    Bozoklar, R.3    Ozkinay, F.4
  • 5
    • 0017726811 scopus 로고
    • Prenatal diagnosis of genetic diseases
    • EPSTEIN C.J., GOLBUS M.S.: Prenatal diagnosis of genetic diseases. Am. Sci., 1977, 65, 703-711.
    • (1977) Am. Sci. , vol.65 , pp. 703-711
    • Epstein, C.J.1    Golbus, M.S.2
  • 7
    • 0027174623 scopus 로고
    • Genetic amniocentesis: A six-years experience in an isolated region of northeastern Quebec (Canada)
    • HAMEL G., SIMARD L., GAGNE R., DE BRAEKELEER M.: Genetic amniocentesis: a six-years experience in an isolated region of northeastern Quebec (Canada). Genet. Counsel., 1993, 4, 103-108.
    • (1993) Genet. Counsel. , vol.4 , pp. 103-108
    • Hamel, G.1    Simard, L.2    Gagne, R.3    De Braekeleer, M.4
  • 8
    • 0020696212 scopus 로고
    • Chromosomal abnormality rates at amniocentesis and in live-born infants
    • HOOK E.B., CROSS P.K., SCHREINEMACHERS D.M.: Chromosomal abnormality rates at amniocentesis and in live-born infants. JAMA, 1983, 249, 2034-2038.
    • (1983) JAMA , vol.249 , pp. 2034-2038
    • Hook, E.B.1    Cross, P.K.2    Schreinemachers, D.M.3
  • 11
    • 0016713786 scopus 로고
    • A clinical service for prenatal diagnosis
    • LAXOVA R., LEWIS B. V., SUDDABY M.: A clinical service for prenatal diagnosis. Lancet, 1975, 2, 964-966.
    • (1975) Lancet , vol.2 , pp. 964-966
    • Laxova, R.1    Lewis, B.V.2    Suddaby, M.3
  • 12
    • 0026770975 scopus 로고
    • Canadian multicentre randomized clinical trial of chorion villus sampling and amniocentesis
    • LIPPMAN A., TOMKINS D.J., SHIME J., HAMERTON J.L.: Canadian multicentre randomized clinical trial of chorion villus sampling and amniocentesis. Prenat. Diagn., 1992, 12, 385-476.
    • (1992) Prenat. Diagn. , vol.12 , pp. 385-476
    • Lippman, A.1    Tomkins, D.J.2    Shime, J.3    Hamerton, J.L.4
  • 13
    • 0342828784 scopus 로고
    • Amniocentesis
    • D.J.H. Brock, C.H. Rodeck, M.A. Ferguson-Smith (eds). Hong Kong, Churchill Livingstone
    • MAC LACHLAN N.A.: Amniocentesis. In: Prenatal Diagnosis and Screening. D.J.H. Brock, C.H. Rodeck, M.A. Ferguson-Smith (eds). Hong Kong, Churchill Livingstone. 1992, 13-21.
    • (1992) Prenatal Diagnosis and Screening , pp. 13-21
    • Mac Lachlan, N.A.1
  • 14
    • 0025665386 scopus 로고
    • Prenatal diagnosis of chromosome abnormalities
    • MURER-ORLANDO M., ZAHED L., DOCHERTY Z.: Prenatal diagnosis of chromosome abnormalities. Genetica, 1990, 83, 61-65.
    • (1990) Genetica , vol.83 , pp. 61-65
    • Murer-Orlando, M.1    Zahed, L.2    Docherty, Z.3
  • 15
    • 0032480524 scopus 로고    scopus 로고
    • Trends in prenatal screening for and diagnosis of Down's syndrome, England and Wales, 1989-97
    • MUTTON D., IDE R.G., ALBERMAN E.: Trends in prenatal screening for and diagnosis of Down's syndrome, England and Wales, 1989-97. BMJ, 1998, 317, 922-923.
    • (1998) BMJ , vol.317 , pp. 922-923
    • Mutton, D.1    Ide, R.G.2    Alberman, E.3
  • 16
    • 0023086246 scopus 로고
    • Temporal changes in Ohio amniocentesis utilization during the first twelve years (1972-1983), and frequency of chromosome abnormalities observed
    • NABER J.M., HUETHER C.A., GOODWIN B.A.: Temporal changes in Ohio amniocentesis utilization during the first twelve years (1972-1983), and frequency of chromosome abnormalities observed. Prenat. Diagn., 1987, 7, 51-65.
    • (1987) Prenat. Diagn. , vol.7 , pp. 51-65
    • Naber, J.M.1    Huether, C.A.2    Goodwin, B.A.3
  • 17
    • 0031467063 scopus 로고    scopus 로고
    • Trends in the use of prenatal diagnosis in New York State and the impact of biochemical screening on the detection of Down syndrome, 1984-1993
    • OLSEN C.L., CROSS P.K.: Trends in the use of prenatal diagnosis in New York State and the impact of biochemical screening on the detection of Down syndrome, 1984-1993. Prenat. Diagn., 1997, 17, 1113-1124.
    • (1997) Prenat. Diagn. , vol.17 , pp. 1113-1124
    • Olsen, C.L.1    Cross, P.K.2
  • 18
    • 0036167673 scopus 로고    scopus 로고
    • A negative second trimester triple test and absence of specific ultrasonographic markers may decrease the need for genetic amniocentesis in advanced maternal age by 60%
    • ROSEN D.J., KEDAR I., AMIEL A., BEN-TOVIM T., PETEL Y., KANETI H., TOHAR M., FEJGIN M.D.: A negative second trimester triple test and absence of specific ultrasonographic markers may decrease the need for genetic amniocentesis in advanced maternal age by 60%. Prenat. Diagn., 2002, 22, 59-63.
    • (2002) Prenat. Diagn. , vol.22 , pp. 59-63
    • Rosen, D.J.1    Kedar, I.2    Amiel, A.3    Ben-Tovim, T.4    Petel, Y.5    Kaneti, H.6    Tohar, M.7    Fejgin, M.D.8
  • 20
    • 0014021719 scopus 로고
    • Chromosome analysis of human fluid cells
    • STEELE M.W., BREG W.R.: Chromosome analysis of human fluid cells. Lancet, 1966, 1, 383-385.
    • (1966) Lancet , vol.1 , pp. 383-385
    • Steele, M.W.1    Breg, W.R.2
  • 21
    • 0028716799 scopus 로고
    • Prenatal diagnosis in Canada-1990. A review
    • STRANC L.C., EVANS J.A., HAMERTON J.L.: Prenatal diagnosis in Canada-1990. A review. Prenat. Diagn., 1994, 14, 1253-1255.
    • (1994) Prenat. Diagn. , vol.14 , pp. 1253-1255
    • Stranc, L.C.1    Evans, J.A.2    Hamerton, J.L.3
  • 22
    • 0029562541 scopus 로고
    • Early amniocentesis. A clinical review
    • WILSON R.D.: Early amniocentesis, A clinical review. Prenat. Diagn., 1995, 15, 1259-1273.
    • (1995) Prenat. Diagn. , vol.15 , pp. 1259-1273
    • Wilson, R.D.1
  • 24
    • 0025878982 scopus 로고
    • Single-center comparison of results of 1000 prenatal diagnoses with chorionic villus sampling and 1000 diagnoses with amniocentesis
    • YOUNG S.R., SHIPLEY C.F., WADE R.V., EDWARDS J.G., WATERS M.B., CANTU M.L., BEST R.G., DENIS E.J.: Single-center comparison of results of 1000 prenatal diagnoses with chorionic villus sampling and 1000 diagnoses with amniocentesis. Am. J. Obstet. Gynecol., 1991, 165, 255-263.
    • (1991) Am. J. Obstet. Gynecol. , vol.165 , pp. 255-263
    • Young, S.R.1    Shipley, C.F.2    Wade, R.V.3    Edwards, J.G.4    Waters, M.B.5    Cantu, M.L.6    Best, R.G.7    Denis, E.J.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.