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Volumn 38, Issue 4, 2011, Pages 364-368

Evaluation of clinical and cytogenetic findings on 1,068 second-trimester amniocenteses in Southeast Turkey

Author keywords

Amniocentesis; Chromosome aberrations; Genetic counseling; Prenatal diagnosis

Indexed keywords

ADULT; AMNIOCENTESIS; ARTICLE; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME INVERSION; CLINICAL EVALUATION; CYTOGENETICS; FEMALE; GENETIC COUNSELING; HUMAN; HUMAN TISSUE; KARYOTYPE; KLINEFELTER SYNDROME; MATERNAL AGE; MATERNAL SERUM; PRENATAL DIAGNOSIS; RECIPROCAL CHROMOSOME TRANSLOCATION; ROBERTSONIAN CHROMOSOME TRANSLOCATION; SECOND TRIMESTER PREGNANCY; TISSUE CULTURE; TRIPLOIDY; TRISOMY; TRISOMY 18; TRISOMY 21; TURKEY (REPUBLIC); TURNER SYNDROME; EVALUATION; MULTIPLE MALFORMATION SYNDROME; PREDICTIVE VALUE; PREGNANCY; PREGNANCY OUTCOME; STATISTICS;

EID: 84856978877     PISSN: 03906663     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (8)

References (28)
  • 3
  • 5
  • 7
    • 79959748788 scopus 로고    scopus 로고
    • The results of second trimester genetic amniocentesis procedure: Adnan menderes University Experience with the results of 22 Centers in Turkey
    • Odabasi A.R., Yüksel H., Demircan S., Temocin K., Bal F., Yapici S. et al.: "The results of second trimester genetic amniocentesis procedure: adnan menderes University Experience with the results of 22 Centers in Turkey". Turkiye Klinikleri J. Gynecol. Obstet., 2007, 17, 196.
    • (2007) Turkiye Klinikleri J. Gynecol. Obstet. , vol.17 , pp. 196
    • Odabasi, A.R.1    Yüksel, H.2    Demircan, S.3    Temocin, K.4    Bal, F.5    Yapici, S.6
  • 8
    • 33645735489 scopus 로고    scopus 로고
    • Detection of chromosome aberrations in the second trimester using genetic amniocentesis: Experience during 1995-2004
    • Tseng J.J., Chou M.M., Lo F.C., Lai H.Y., Chen M.H., Ho E.S.: "Detection of chromosome aberrations in the second trimester using genetic amniocentesis: experience during 1995-2004". Taiwan J. Obstet. Gynecol., 2006, 45, 39.
    • (2006) Taiwan J. Obstet. Gynecol. , vol.45 , pp. 39
    • Tseng, J.J.1    Chou, M.M.2    Lo, F.C.3    Lai, H.Y.4    Chen, M.H.5    Ho, E.S.6
  • 9
    • 33748283130 scopus 로고    scopus 로고
    • Cytogenetic results of amniocentesis materials: Incidence of abnormal karyotypes in the Turkish collaborative study
    • Karaoguz M.Y., Bal F., Yakut T., Ercelen N.O., Ergun M.A., Gokcen A.B. et al.: "Cytogenetic results of amniocentesis materials: incidence of abnormal karyotypes in the Turkish collaborative study". Genet. Couns., 2006, 17, 219.
    • (2006) Genet. Couns. , vol.17 , pp. 219
    • Karaoguz, M.Y.1    Bal, F.2    Yakut, T.3    Ercelen, N.O.4    Ergun, M.A.5    Gokcen, A.B.6
  • 10
    • 12944302599 scopus 로고    scopus 로고
    • Second-trimester genetic amniocentesis: 5-Year experience
    • Turhan N.O., Eren U., Seckin N.C.: "Second-trimester genetic amniocentesis: 5-year experience". Arch. Gynecol. Obstet., 2005, 271, 19.
    • (2005) Arch. Gynecol. Obstet. , vol.271 , pp. 19
    • Turhan, N.O.1    Eren, U.2    Seckin, N.C.3
  • 11
    • 12144289745 scopus 로고    scopus 로고
    • Trends in cytogenetic prenatal diagnosis in a reference hospital in Izmir/Turkey: A comparative study for four years
    • Gunduz C., Cogulu O., Cankaya T., Bora E., Karaca E., Alpman A. et al.: "Trends in cytogenetic prenatal diagnosis in a reference hospital in Izmir/Turkey: a comparative study for four years". Genet. Couns., 2004, 15, 53.
    • (2004) Genet. Couns. , vol.15 , pp. 53
    • Gunduz, C.1    Cogulu, O.2    Cankaya, T.3    Bora, E.4    Karaca, E.5    Alpman, A.6
  • 12
  • 13
    • 0035379981 scopus 로고    scopus 로고
    • Frequencies of fetal chromosomal abnormalities at prenatal diagnosis: 10 Years experiences in a single institution
    • Park S.Y., Kim J.W., Kim Y.M., Lee M.H., Lee B.Y. et al.: "Frequencies of fetal chromosomal abnormalities at prenatal diagnosis: 10 years experiences in a single institution". J. Korean Med. Sci., 2001, 16, 290.
    • (2001) J. Korean Med. Sci. , vol.16 , pp. 290
    • Park, S.Y.1    Kim, J.W.2    Kim, Y.M.3    Lee, M.H.4    Lee, B.Y.5
  • 14
    • 0033203060 scopus 로고    scopus 로고
    • The Korean collaborative study on 11,000 prenatal genetic amniocentesis
    • Yang Y.H., Ju K.S., Kim S.B., Cho Y.H., Lee J.H., Lee S.H. et al.: "The Korean collaborative study on 11,000 prenatal genetic amniocentesis". Yonsei Med. J., 1999, 40, 460.
    • (1999) Yonsei Med. J. , vol.40 , pp. 460
    • Yang, Y.H.1    Ju, K.S.2    Kim, S.B.3    Cho, Y.H.4    Lee, J.H.5    Lee, S.H.6
  • 15
    • 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. Gene., 1999, 82, 149.
    • (1999) Am. J. Med. Gene. , vol.82 , pp. 149
    • Caron, L.1    Tihy, F.2    Dallaire, L.3
  • 16
    • 0024442164 scopus 로고
    • A decade of mid-trimester amniocentesis in Johannesburg. Prenatal diagnosis, problems and counselling
    • Kromberg J.G., Bernstein R., Jacobson M.J., Rosendorff J., Jenkins T.: "A decade of mid-trimester amniocentesis in Johannesburg. Prenatal diagnosis, problems and counselling". S. Afr. Med. J., 1989, 76, 344.
    • (1989) S. Afr. Med. J. , vol.76 , pp. 344
    • Kromberg, J.G.1    Bernstein, R.2    Jacobson, M.J.3    Rosendorff, J.4    Jenkins, T.5
  • 19
    • 77954454400 scopus 로고    scopus 로고
    • Cytogenetic analysis of 4216 patients referred for suspected chromosomal abnormalities in Southeast Turkey
    • Balkan M., Akbas H., Isi H., Oral D., Turkyilmaz A., Kalkanli S. et al.: "Cytogenetic analysis of 4216 patients referred for suspected chromosomal abnormalities in Southeast Turkey". Genet. Mol. Res., 2010, 11, 1094.
    • (2010) Genet. Mol. Res. , vol.11 , pp. 1094
    • Balkan, M.1    Akbas, H.2    Isi, H.3    Oral, D.4    Turkyilmaz, A.5    Kalkanli, S.6
  • 20
    • 62549102871 scopus 로고    scopus 로고
    • Prenatal diagnosis of fetal chromosomal abnormalities: Report of an 18-year experience in a Brazilian public hospital
    • Kessler R.G., Sanseverino M.T.V., Leistner-Segal S., Magalhães J.A.A., Giugliani R.: "Prenatal diagnosis of fetal chromosomal abnormalities: Report of an 18-year experience in a Brazilian public hospital". Gen. Mol. Biol., 2008, 31, 829.
    • (2008) Gen. Mol. Biol. , vol.31 , pp. 829
    • Kessler, R.G.1    Sanseverino, M.T.V.2    Leistner-Segal, S.3    Magalhães, J.A.A.4    Giugliani, R.5
  • 21
    • 0030884507 scopus 로고    scopus 로고
    • Transplacental needle passage and other risk factors associated with second trimester amniocentesis
    • Marthin T., Liedgren S., Hammar M.: "Transplacental needle passage and other risk factors associated with second trimester amniocentesis". Acta Obstet. Gynecol. Scand., 1997, 76, 728.
    • (1997) Acta Obstet. Gynecol. Scand. , vol.76 , pp. 728
    • Marthin, T.1    Liedgren, S.2    Hammar, M.3
  • 23
    • 80054706318 scopus 로고    scopus 로고
    • Results of amniocentesis in 7 years period in Eskisehir Osmangazi University
    • Sener K.T., Durak B., Tanir H.M., Tepeli E., Kaya M., Artan S.: "Results of amniocentesis in 7 years period in Eskisehir Osmangazi University". Perinatol., 2006, 14, 170.
    • (2006) Perinatol. , vol.14 , pp. 170
    • Sener, K.T.1    Durak, B.2    Tanir, H.M.3    Tepeli, E.4    Kaya, M.5    Artan, S.6
  • 24
    • 33646051217 scopus 로고    scopus 로고
    • Second-trimester prenatal screening for trisomy 21 using biochemical markers: A 7-year experience in one cytogenetic laboratory
    • Marical H., Douet-Guilbert N., Bages K., Collet M., Le Bris M.J., Morel F. et al.: "Second-trimester prenatal screening for trisomy 21 using biochemical markers: a 7-year experience in one cytogenetic laboratory". Prenat. Diagn., 2006, 26, 308.
    • (2006) Prenat. Diagn. , vol.26 , pp. 308
    • Marical, H.1    Douet-Guilbert, N.2    Bages, K.3    Collet, M.4    Le Bris, M.J.5    Morel, F.6
  • 25
    • 33947390489 scopus 로고    scopus 로고
    • Parental decisions to abort or continue a pregnancy following prenatal diagnosis of chromosomal abnormalities in a setting where termination of pregnancy is not legally available
    • Quadrelli R., Quadrelli A., Mechoso B., Laufer M., Jaumandreu C., Vaglio A.: "Parental decisions to abort or continue a pregnancy following prenatal diagnosis of chromosomal abnormalities in a setting where termination of pregnancy is not legally available". Prenatal. Diagnosis, 2007, 27, 228.
    • (2007) Prenatal. Diagnosis , vol.27 , pp. 228
    • Quadrelli, R.1    Quadrelli, A.2    Mechoso, B.3    Laufer, M.4    Jaumandreu, C.5    Vaglio, A.6
  • 27
    • 0033174755 scopus 로고    scopus 로고
    • Chromosome abnormalities in a referred population for suspected chromosomal aberrations: A report of 4117 cases
    • Kim S.S., Jung S.C., Kim H.J., Moon H.R., Lee J.S.: "Chromosome abnormalities in a referred population for suspected chromosomal aberrations: a report of 4117 cases". J. Korean Med. Sci., 1999, 14, 373.
    • (1999) J. Korean Med. Sci. , vol.14 , pp. 373
    • Kim, S.S.1    Jung, S.C.2    Kim, H.J.3    Moon, H.R.4    Lee, J.S.5
  • 28
    • 0027073145 scopus 로고
    • Population studies of INV(9) chromosomes in 4,300 Japanese: Incidence, sex difference and clinical significance
    • Yamada K.: "Population studies of INV(9) chromosomes in 4,300 Japanese: incidence, sex difference and clinical significance". Jpn. J. Hum. Genet., 1992, 37, 293.
    • (1992) Jpn. J. Hum. Genet. , vol.37 , pp. 293
    • Yamada, K.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.