메뉴 건너뛰기




Volumn 49, Issue 1, 2010, Pages 120-123

Rapid Genome-wide Aneuploidy Diagnosis Using Uncultured Amniocytes and Array Comparative Genomic Hybridization in Pregnancy With Abnormal Ultrasound Findings Detected in Late Second and Third Trimesters

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AMNIOCENTESIS; AMNION CELL; AMNION FLUID ANALYSIS; ANAMNESIS; ANEUPLOIDY; BACTERIAL ARTIFICIAL CHROMOSOME; BRAIN MALFORMATION; BRAIN VENTRICLE DILATATION; CASE REPORT; COMPARATIVE GENOMIC HYBRIDIZATION; CYTOGENETICS; DOWN SYNDROME; ECHOCARDIOGRAPHY; FEMALE; FETAL BIOPHYSICAL PROFILE; FETUS HEART; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC ASSOCIATION; HEART DISEASE; HUMAN; KARYOTYPE; LETTER; MEIOSIS; MENTAL DEFICIENCY; NEWBORN; POLYMERASE CHAIN REACTION; PREGNANCY DISORDER; PRENATAL DIAGNOSIS; QUANTITATIVE STUDY; RANDOM AMPLIFIED POLYMORPHIC DNA; RELATIVE; THIRD TRIMESTER PREGNANCY; TRISOMY 21;

EID: 77953266539     PISSN: 10284559     EISSN: 10284559     Source Type: Journal    
DOI: 10.1016/S1028-4559(10)60026-5     Document Type: Letter
Times cited : (10)

References (30)
  • 1
    • 77949498680 scopus 로고    scopus 로고
    • 22q11.2 microdeletion in a fetus with double-outlet right ventricle, pulmonary stenosis and a ventricular septal defect: prenatal diagnosis by array comparative genomic hybridization
    • Chen C.P., Su Y.N., Chang T.Y., Chern S.R., Tsai F.J., Hwang J.K., and Wang W. 22q11.2 microdeletion in a fetus with double-outlet right ventricle, pulmonary stenosis and a ventricular septal defect: prenatal diagnosis by array comparative genomic hybridization. Taiwan J Obstet Gynecol 48 (2009) 437-440
    • (2009) Taiwan J Obstet Gynecol , vol.48 , pp. 437-440
    • Chen, C.P.1    Su, Y.N.2    Chang, T.Y.3    Chern, S.R.4    Tsai, F.J.5    Hwang, J.K.6    Wang, W.7
  • 2
    • 77949498196 scopus 로고    scopus 로고
    • Terminal 2q deletion and distal 15q duplication: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes
    • Chen C.P., Su Y.N., Tsai F.J., et al. Terminal 2q deletion and distal 15q duplication: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes. Taiwan J Obstet Gynecol 48 (2009) 441-445
    • (2009) Taiwan J Obstet Gynecol , vol.48 , pp. 441-445
    • Chen, C.P.1    Su, Y.N.2    Tsai, F.J.3
  • 3
    • 0029160412 scopus 로고
    • CDC publishes report on chorionic villus sampling and amniocentesis
    • CDC publishes report on chorionic villus sampling and amniocentesis. Am Fam Physician 52 (1995) 1210
    • (1995) Am Fam Physician , vol.52 , pp. 1210
  • 4
    • 0029649790 scopus 로고
    • Chorionic vil-lus sampling and amniocentesis: recommendations for prenatal counseling
    • Centers for Disease Control and Prevention. Chorionic vil-lus sampling and amniocentesis: recommendations for prenatal counseling. MMWR Recomm Rep 44 (1995) 1-12
    • (1995) MMWR Recomm Rep , vol.44 , pp. 1-12
    • Centers for Disease Control and Prevention1
  • 5
    • 0022361136 scopus 로고
    • Fetal blood sampling during pregnancy with use of a needle guided by ultrasound: a study of 606 consecutive cases
    • Daffos F., Capella-Pavlovsky M., and Forestier F. Fetal blood sampling during pregnancy with use of a needle guided by ultrasound: a study of 606 consecutive cases. Am J Obstet Gynecol 153 (1985) 655-660
    • (1985) Am J Obstet Gynecol , vol.153 , pp. 655-660
    • Daffos, F.1    Capella-Pavlovsky, M.2    Forestier, F.3
  • 6
    • 0025777692 scopus 로고
    • Fetal blood sampling from the intrahepatic vein for rapid karyotyping in the second and third trimesters
    • Nicolaidis P., Nicolini U., Fisk N.M., Tannirandorn Y., Nasrat H., and Rodeck C.H. Fetal blood sampling from the intrahepatic vein for rapid karyotyping in the second and third trimesters. Br J Radiol 64 (1991) 505-509
    • (1991) Br J Radiol , vol.64 , pp. 505-509
    • Nicolaidis, P.1    Nicolini, U.2    Fisk, N.M.3    Tannirandorn, Y.4    Nasrat, H.5    Rodeck, C.H.6
  • 7
    • 0029982004 scopus 로고    scopus 로고
    • Diagnostic fetal blood sampling-technique related losses
    • Weiner C.P., and Okamura K. Diagnostic fetal blood sampling-technique related losses. Fetal Diagn Ther 11 (1996) 169-175
    • (1996) Fetal Diagn Ther , vol.11 , pp. 169-175
    • Weiner, C.P.1    Okamura, K.2
  • 11
    • 0035081439 scopus 로고    scopus 로고
    • A large-scale evaluation of amnio-PCR for the rapid prenatal diagnosis of fetal tri-somy
    • Levett L.J., Liddle S., and Meredith R. A large-scale evaluation of amnio-PCR for the rapid prenatal diagnosis of fetal tri-somy. Ultrasound Obstet Gynecol 17 (2001) 115-118
    • (2001) Ultrasound Obstet Gynecol , vol.17 , pp. 115-118
    • Levett, L.J.1    Liddle, S.2    Meredith, R.3
  • 12
    • 0035968604 scopus 로고    scopus 로고
    • Development and implementation of a new rapid aneuploidy diagnostic service within the UK National Health Service and implications for the future of prenatal diagnosis
    • Mann K., Fox S.P., Abbs S.J., Yau S.C., Scriven P.N., Docherty Z., and Ogilvie C.M. Development and implementation of a new rapid aneuploidy diagnostic service within the UK National Health Service and implications for the future of prenatal diagnosis. Lancet 358 (2001) 1057-1061
    • (2001) Lancet , vol.358 , pp. 1057-1061
    • Mann, K.1    Fox, S.P.2    Abbs, S.J.3    Yau, S.C.4    Scriven, P.N.5    Docherty, Z.6    Ogilvie, C.M.7
  • 13
    • 0036107146 scopus 로고    scopus 로고
    • Prenatal diagnosis of common aneuploidies using quantitative fluorescent PCR
    • Bili C., Divane A., Apessos A., et al. Prenatal diagnosis of common aneuploidies using quantitative fluorescent PCR. Prenat Diagn 22 (2002) 360-365
    • (2002) Prenat Diagn , vol.22 , pp. 360-365
    • Bili, C.1    Divane, A.2    Apessos, A.3
  • 14
    • 19944407550 scopus 로고    scopus 로고
    • Rapid prenatal diagnosis of common chromosome aneuploidies by QF-PCR: assessment on 18,000 consecutive clinical samples
    • Cirigliano V., Voglino G., Cañadas M.P., et al. Rapid prenatal diagnosis of common chromosome aneuploidies by QF-PCR: assessment on 18,000 consecutive clinical samples. Mol Hum Reprod 10 (2004) 839-846
    • (2004) Mol Hum Reprod , vol.10 , pp. 839-846
    • Cirigliano, V.1    Voglino, G.2    Cañadas, M.P.3
  • 15
    • 33749573864 scopus 로고    scopus 로고
    • Rapid prenatal diagnosis by QF-PCR: evaluation of 30,000 consecutive clinical samples and future applications
    • Cirigliano V., Voglino G., Marongiu A., et al. Rapid prenatal diagnosis by QF-PCR: evaluation of 30,000 consecutive clinical samples and future applications. Ann N Y Acad Sci 1075 (2006) 288-298
    • (2006) Ann N Y Acad Sci , vol.1075 , pp. 288-298
    • Cirigliano, V.1    Voglino, G.2    Marongiu, A.3
  • 17
    • 33645778232 scopus 로고    scopus 로고
    • Prenatal detection of unbalanced chromosomal rearrangements by array CGH
    • Rickman L., Fiegler H., Shaw-Smith C., et al. Prenatal detection of unbalanced chromosomal rearrangements by array CGH. J Med Genet 43 (2006) 353-361
    • (2006) J Med Genet , vol.43 , pp. 353-361
    • Rickman, L.1    Fiegler, H.2    Shaw-Smith, C.3
  • 18
    • 33751172713 scopus 로고    scopus 로고
    • Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization
    • Sahoo T., Cheung S.W., Ward P., et al. Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization. Genet Med 8 (2006) 719-727
    • (2006) Genet Med , vol.8 , pp. 719-727
    • Sahoo, T.1    Cheung, S.W.2    Ward, P.3
  • 19
    • 33646521074 scopus 로고    scopus 로고
    • Comparative genomic hybridization and prenatal diagnosis
    • van den Veyver I.B., and Beaudet A.L. Comparative genomic hybridization and prenatal diagnosis. Curr Opin Obstet Gynecol 18 (2006) 185-191
    • (2006) Curr Opin Obstet Gynecol , vol.18 , pp. 185-191
    • van den Veyver, I.B.1    Beaudet, A.L.2
  • 20
    • 33947237911 scopus 로고    scopus 로고
    • Molecular cytogenetic and rapid aneuploidy detection methods in prenatal diagnosis
    • Shaffer L.G., and Bui T.H. Molecular cytogenetic and rapid aneuploidy detection methods in prenatal diagnosis. Am J Med Genet C Semin Med Genet 145C (2007) 87-98
    • (2007) Am J Med Genet C Semin Med Genet , vol.145 C , pp. 87-98
    • Shaffer, L.G.1    Bui, T.H.2
  • 21
    • 55449108848 scopus 로고    scopus 로고
    • Rapid prenatal diagnosis using uncultured amniocytes and oligonucleotide array CGH
    • Bi W., Breman A.M., Venable S.F., et al. Rapid prenatal diagnosis using uncultured amniocytes and oligonucleotide array CGH. Prenat Diagn 28 (2008) 943-949
    • (2008) Prenat Diagn , vol.28 , pp. 943-949
    • Bi, W.1    Breman, A.M.2    Venable, S.F.3
  • 22
    • 52349090477 scopus 로고    scopus 로고
    • Prenatal detection of a subtle unbalanced chromosome rearrangement by karyotyping, FISH and array comparative genomic hybridization
    • Cain C.C., Saul D.O., Oehler E., Blakemore K., and Stetten G. Prenatal detection of a subtle unbalanced chromosome rearrangement by karyotyping, FISH and array comparative genomic hybridization. Fetal Diagn Ther 24 (2008) 286-290
    • (2008) Fetal Diagn Ther , vol.24 , pp. 286-290
    • Cain, C.C.1    Saul, D.O.2    Oehler, E.3    Blakemore, K.4    Stetten, G.5
  • 23
    • 38149038032 scopus 로고    scopus 로고
    • Pre- and postnatal genetic testing by array-comparative genomic hybridization: genetic counseling perspectives
    • Darilek S., Ward P., Pursley A., et al. Pre- and postnatal genetic testing by array-comparative genomic hybridization: genetic counseling perspectives. Genet Med 10 (2008) 13-18
    • (2008) Genet Med , vol.10 , pp. 13-18
    • Darilek, S.1    Ward, P.2    Pursley, A.3
  • 25
    • 77953233752 scopus 로고    scopus 로고
    • Prenatal diagnosis by array-based comparative genomic hybridization in the clinical laboratory setting
    • Breman A.M., Bi W.M., and Cheung S.W. Prenatal diagnosis by array-based comparative genomic hybridization in the clinical laboratory setting. Beijing Da Xue Xue Bao 41 (2009) 500-504
    • (2009) Beijing Da Xue Xue Bao , vol.41 , pp. 500-504
    • Breman, A.M.1    Bi, W.M.2    Cheung, S.W.3
  • 27
    • 66749178395 scopus 로고    scopus 로고
    • Array comparative genomic hybridization in prenatal diagnosis: another experience
    • Vialard F., Molina Gomes D., Leroy B., et al. Array comparative genomic hybridization in prenatal diagnosis: another experience. Fetal Diagn Ther 25 (2009) 277-284
    • (2009) Fetal Diagn Ther , vol.25 , pp. 277-284
    • Vialard, F.1    Molina Gomes, D.2    Leroy, B.3
  • 28
    • 33845274890 scopus 로고    scopus 로고
    • Detection of low-level mosaicism by array CGH in routine diagnostic specimens
    • Ballif B.C., Rorem E.A., Sundin K., et al. Detection of low-level mosaicism by array CGH in routine diagnostic specimens. Am J Med Genet A 140 (2006) 2757-2767
    • (2006) Am J Med Genet A , vol.140 , pp. 2757-2767
    • Ballif, B.C.1    Rorem, E.A.2    Sundin, K.3
  • 29
    • 34547697696 scopus 로고    scopus 로고
    • Microarray-based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics
    • Cheung S.W., Shaw C.A., Scott D.A., et al. Microarray-based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics. Am J Med Genet A 143 (2007) 1679-1686
    • (2007) Am J Med Genet A , vol.143 , pp. 1679-1686
    • Cheung, S.W.1    Shaw, C.A.2    Scott, D.A.3
  • 30
    • 44449112745 scopus 로고    scopus 로고
    • Low-level mosaicism of trisomy 14: phenotypic and molecular characterization
    • Shinawi M., Shao L., Jeng L.J., et al. Low-level mosaicism of trisomy 14: phenotypic and molecular characterization. Am J Med Genet A 146 (2008) 1395-1405
    • (2008) Am J Med Genet A , vol.146 , pp. 1395-1405
    • Shinawi, M.1    Shao, L.2    Jeng, L.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.