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Volumn 33, Issue 4, 2013, Pages 371-377

Prenatal chromosomal microarray analysis: A survey of prenatal genetic counselors' experiences and attitudes

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGE DISTRIBUTION; ARTICLE; CANADA; CHROMOSOMAL MICROARRAY ANALYSIS; CONTROLLED STUDY; DIAGNOSTIC ACCURACY; FEMALE; GENETIC COUNSELING; HUMAN; MAJOR CLINICAL STUDY; MICROARRAY ANALYSIS; OPEN-ENDED QUESTIONNAIRE; PRENATAL CARE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; UNITED STATES; VOCATIONAL GUIDANCE;

EID: 84875653819     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.4071     Document Type: Article
Times cited : (22)

References (29)
  • 1
    • 34249717942 scopus 로고    scopus 로고
    • Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases
    • Lu X, Shaw CA, Patel A, et al. Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases. PLoS ONE 2007;2:e327.
    • (2007) PLoS ONE , vol.2
    • Lu, X.1    Shaw, C.A.2    Patel, A.3
  • 3
    • 84866999347 scopus 로고    scopus 로고
    • Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies
    • Shaffer LG, Dabell MP, Fisher AJ, et al. Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies. Prenat Diagn 2012;32:976-85.
    • (2012) Prenat Diagn , vol.32 , pp. 976-985
    • Shaffer, L.G.1    Dabell, M.P.2    Fisher, A.J.3
  • 4
    • 78649635514 scopus 로고    scopus 로고
    • Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities
    • Manning M, Hudgins L. Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities. Genet Med 2010;12:742-5.
    • (2010) Genet Med , vol.12 , pp. 742-745
    • Manning, M.1    Hudgins, L.2
  • 5
    • 77952032690 scopus 로고    scopus 로고
    • Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies
    • Miller DT, Adam MP, Aradhya S, et al. Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. Am J Hum Genet 2010;86:749-64.
    • (2010) Am J Hum Genet , vol.86 , pp. 749-764
    • Miller, D.T.1    Adam, M.P.2    Aradhya, S.3
  • 6
    • 73549121749 scopus 로고    scopus 로고
    • ACOG Committee Opinion No. 446: array comparative genomic hybridization in prenatal diagnosis
    • American College of Obstetricians and Gynecologists Committee.
    • American College of Obstetricians and Gynecologists Committee. ACOG Committee Opinion No. 446: array comparative genomic hybridization in prenatal diagnosis. Obstet Gynecol 2009;114:1161-3.
    • (2009) Obstet Gynecol , vol.114 , pp. 1161-1163
  • 7
    • 84875659863 scopus 로고    scopus 로고
    • Canadian College of Medical Geneticists Cytogenetics Committee. Ottawa, Canada: Canadian College of Medical Geneticists;
    • Canadian College of Medical Geneticists Cytogenetics Committee. CCMG Guidelines for Genomic Microarray Testing. Ottawa, Canada: Canadian College of Medical Geneticists; 2010. p. 1-10.
    • (2010) CCMG Guidelines for Genomic Microarray Testing , pp. 1-10
  • 8
    • 78650632807 scopus 로고    scopus 로고
    • Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis
    • Hillman SC, Pretlove S, Coomarasamy A, et al. Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis. Ultrasound Obstet Gynecol 2011;37:6-14.
    • (2011) Ultrasound Obstet Gynecol , vol.37 , pp. 6-14
    • Hillman, S.C.1    Pretlove, S.2    Coomarasamy, A.3
  • 9
    • 84870549609 scopus 로고    scopus 로고
    • Chromosomal microarray versus karyotyping for prenatal diagnosis
    • Wapner RJ, Martin CL, Levy B, et al. Chromosomal microarray versus karyotyping for prenatal diagnosis. N Engl J Med 2012;367:2175-84.
    • (2012) N Engl J Med , vol.367 , pp. 2175-2184
    • Wapner, R.J.1    Martin, C.L.2    Levy, B.3
  • 10
    • 59449102851 scopus 로고    scopus 로고
    • Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases
    • Van den Veyver IB, Patel A, Shaw CA, et al. Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases. Prenat Diagn 2009;29:29-39.
    • (2009) Prenat Diagn , vol.29 , pp. 29-39
    • Van den Veyver, I.B.1    Patel, A.2    Shaw, C.A.3
  • 11
    • 13444287933 scopus 로고    scopus 로고
    • Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations
    • Le Caignec C, Boceno M, Saugier-Veber P, et al. Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations. J Med Genet 2005;42:121-8.
    • (2005) J Med Genet , vol.42 , pp. 121-128
    • Le Caignec, C.1    Boceno, M.2    Saugier-Veber, P.3
  • 12
    • 77954932491 scopus 로고    scopus 로고
    • Evaluation of array comparative genomic hybridization for genetic analysis of chorionic villus sampling from pregnancy loss in comparison to karyotyping and multiplex ligation-dependent probe amplification
    • Deshpande M, Harper J, Holloway M, et al. Evaluation of array comparative genomic hybridization for genetic analysis of chorionic villus sampling from pregnancy loss in comparison to karyotyping and multiplex ligation-dependent probe amplification. Genet Test Mol Biomarkers 2010;14:421-4.
    • (2010) Genet Test Mol Biomarkers , vol.14 , pp. 421-424
    • Deshpande, M.1    Harper, J.2    Holloway, M.3
  • 13
    • 79953161375 scopus 로고    scopus 로고
    • Evolving applications of microarray analysis in prenatal diagnosis
    • Savage MS, Mourad MJ, Wapner RJ. Evolving applications of microarray analysis in prenatal diagnosis. Curr Opin Obstet Gynecol 2011;23:103-8.
    • (2011) Curr Opin Obstet Gynecol , vol.23 , pp. 103-108
    • Savage, M.S.1    Mourad, M.J.2    Wapner, R.J.3
  • 14
    • 84861478142 scopus 로고    scopus 로고
    • Referral patterns for microarray testing in prenatal diagnosis
    • Shaffer LG, Dabell MP, Rosenfeld JA, et al. Referral patterns for microarray testing in prenatal diagnosis. Prenat Diagn 2012;32:344-50.
    • (2012) Prenat Diagn , vol.32 , pp. 344-350
    • Shaffer, L.G.1    Dabell, M.P.2    Rosenfeld, J.A.3
  • 15
    • 0036153585 scopus 로고    scopus 로고
    • Depressive reactions and stress related to prenatal medicine procedures
    • Kowalcek I, Muhlhoff A, Bachmann S, et al. Depressive reactions and stress related to prenatal medicine procedures. Ultrasound Obstet Gynecol 2002;19:18-23.
    • (2002) Ultrasound Obstet Gynecol , vol.19 , pp. 18-23
    • Kowalcek, I.1    Muhlhoff, A.2    Bachmann, S.3
  • 16
    • 0029418109 scopus 로고
    • Genetic counseling after abnormal prenatal diagnosis: facilitating coping in families who continue their pregnancies
    • Allen JS, Mulhauser LC. Genetic counseling after abnormal prenatal diagnosis: facilitating coping in families who continue their pregnancies. J Genet Couns 1995;4:251-65.
    • (1995) J Genet Couns , vol.4 , pp. 251-265
    • Allen, J.S.1    Mulhauser, L.C.2
  • 17
    • 39749112426 scopus 로고    scopus 로고
    • Anxiety and prenatal testing: do women with soft ultrasound findings have increased anxiety compared to women with other indications for testing?
    • Hoskovec J, Mastrobattista JM, Johnston D, et al. Anxiety and prenatal testing: do women with soft ultrasound findings have increased anxiety compared to women with other indications for testing? Prenat Diagn 2008;28:135-40.
    • (2008) Prenat Diagn , vol.28 , pp. 135-140
    • Hoskovec, J.1    Mastrobattista, J.M.2    Johnston, D.3
  • 18
    • 77956182848 scopus 로고    scopus 로고
    • Triple X syndrome: characteristics of 42 Italian girls and parental emotional response to prenatal diagnosis
    • Lalatta F, Quagliarini D, Folliero E, et al. Triple X syndrome: characteristics of 42 Italian girls and parental emotional response to prenatal diagnosis. Eur J Pediatr 2010;169:1255-61.
    • (2010) Eur J Pediatr , vol.169 , pp. 1255-1261
    • Lalatta, F.1    Quagliarini, D.2    Folliero, E.3
  • 19
    • 0032731315 scopus 로고    scopus 로고
    • Clinical implications of atypical chromosome abnormalities diagnosed prenatally
    • Silver RK, Blum K, Geibel LJ, et al. Clinical implications of atypical chromosome abnormalities diagnosed prenatally. Obstet Gynecol 1999;94:925-8.
    • (1999) Obstet Gynecol , vol.94 , pp. 925-928
    • Silver, R.K.1    Blum, K.2    Geibel, L.J.3
  • 20
    • 33645735489 scopus 로고    scopus 로고
    • Detection of chromosome aberrations in the second trimester using genetic amniocentesis: experience during 1995-2004
    • Tseng JJ, Chou MM, Lo FC, et al. Detection of chromosome aberrations in the second trimester using genetic amniocentesis: experience during 1995-2004. Taiwan J Obstet Gynecol 2006;45:39-41.
    • (2006) Taiwan J Obstet Gynecol , vol.45 , pp. 39-41
    • Tseng, J.J.1    Chou, M.M.2    Lo, F.C.3
  • 21
    • 2442666461 scopus 로고    scopus 로고
    • Prenatal diagnosis of de novo X;autosome translocations
    • Abrams L, Cotter PD. Prenatal diagnosis of de novo X;autosome translocations. Clin Genet 2004;65:423-8.
    • (2004) Clin Genet , vol.65 , pp. 423-428
    • Abrams, L.1    Cotter, P.D.2
  • 23
    • 37649018305 scopus 로고    scopus 로고
    • Advances in missing data methods and implications for educational research
    • In, Sawilowsky SS, ed.). Charlotte, NC: New Information Age Publishing
    • Peng CY, Harwell M, Liou SM, et al. Advances in missing data methods and implications for educational research. In Real Data Analysis, Sawilowsky SS, (ed.). Charlotte, NC: New Information Age Publishing, 2006; 31-78.
    • (2006) Real Data Analysis , pp. 31-78
    • Peng, C.Y.1    Harwell, M.2    Liou, S.M.3
  • 24
    • 84859124052 scopus 로고    scopus 로고
    • Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature
    • Breman A, Pursley AN, Hixson P, et al. Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature. Prenat Diagn 2012;32:351-61.
    • (2012) Prenat Diagn , vol.32 , pp. 351-361
    • Breman, A.1    Pursley, A.N.2    Hixson, P.3
  • 25
    • 84859142327 scopus 로고    scopus 로고
    • Non-targeted whole genome 250K SNP array analysis as replacement for karyotyping in fetuses with structural ultrasound anomalies: evaluation of a one-year experience
    • Faas BH, Feenstra I, Eggink AJ, et al. Non-targeted whole genome 250K SNP array analysis as replacement for karyotyping in fetuses with structural ultrasound anomalies: evaluation of a one-year experience. Prenat Diagn 2012;32:362-70.
    • (2012) Prenat Diagn , vol.32 , pp. 362-370
    • Faas, B.H.1    Feenstra, I.2    Eggink, A.J.3
  • 26
    • 84865123678 scopus 로고    scopus 로고
    • Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: a cohort study of 3171 pregnancies
    • Lee CN, Lin SY, Lin CH, et al. Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: a cohort study of 3171 pregnancies. BJOG: An International Journal of Obstetrics & Gynaecology 2012;119:614-25.
    • (2012) BJOG: An International Journal of Obstetrics & Gynaecology , vol.119 , pp. 614-625
    • Lee, C.N.1    Lin, S.Y.2    Lin, C.H.3
  • 28
    • 84859112155 scopus 로고    scopus 로고
    • Genetic counselling and ethical issues with chromosome microarray analysis in prenatal testing
    • McGillivray G, Rosenfeld JA, McKinlay Gardner RJ, et al. Genetic counselling and ethical issues with chromosome microarray analysis in prenatal testing. Prenat Diagn 2012;32:389-95.
    • (2012) Prenat Diagn , vol.32 , pp. 389-395
    • McGillivray, G.1    Rosenfeld, J.A.2    McKinlay Gardner, R.J.3
  • 29
    • 84859133651 scopus 로고    scopus 로고
    • Integration of microarray technology into prenatal diagnosis: counselling issues generated during the NICHD clinical trial
    • Wapner RJ, Driscoll DA, Simpson JL. Integration of microarray technology into prenatal diagnosis: counselling issues generated during the NICHD clinical trial. Prenat Diagn 2012;32:396-400.
    • (2012) Prenat Diagn , vol.32 , pp. 396-400
    • Wapner, R.J.1    Driscoll, D.A.2    Simpson, J.L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.