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Volumn 32, Issue 7, 2012, Pages 708-709

Array CGH in routine prenatal diagnosis practice

Author keywords

[No Author keywords available]

Indexed keywords

COMPARATIVE GENOMIC HYBRIDIZATION; COPY NUMBER VARIATION; DIAGNOSTIC TEST; FETUS DISEASE; FETUS ECHOGRAPHY; GENETICS; GENOTYPE; HUMAN; LETTER; PHENOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

EID: 84863438703     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.3845     Document Type: Letter
Times cited : (5)

References (7)
  • 1
    • 84863495736 scopus 로고    scopus 로고
    • CDC. Genomic testing, Available at: [accessed on 14 December 2011].
    • CDC. Genomic testing, 2004. Available at: [accessed on 14 December 2011].
    • (2004)
  • 2
    • 82255183120 scopus 로고    scopus 로고
    • Introducing array comparative genomic hybridization into routine prenatal diagnosis practice: a prospective study on over 1000 consecutive cases
    • Fiorentino F, Caiazzo F, Napolitano S, et al. Introducing array comparative genomic hybridization into routine prenatal diagnosis practice: a prospective study on over 1000 consecutive cases. Prenat Diagn 2011;31:1270-82.
    • (2011) Prenat Diagn , vol.31 , pp. 1270-1282
    • Fiorentino, F.1    Caiazzo, F.2    Napolitano, S.3
  • 3
    • 78650632807 scopus 로고    scopus 로고
    • Additional information from array comparative genomic hybridisation 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 hybridisation 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
  • 4
    • 64849105597 scopus 로고    scopus 로고
    • Diagnosis, making the best use of medical data
    • Ebell MH. Diagnosis, making the best use of medical data. Am Fam Physician 2009;79(6):478-80.
    • (2009) Am Fam Physician , vol.79 , Issue.6 , pp. 478-480
    • Ebell, M.H.1
  • 5
    • 84859358210 scopus 로고    scopus 로고
    • Working Group Italian Society of Human Genetics(SIGU) Position Statement. Microarray application in prenatal diagnosis: a position statement from the working group on behalf of the Italian Society of Human Genetics (SIGU), November 2011
    • press, DOI: 10.1002/uog.11092
    • Novelli A, Grati FR, Ballarati L, et al. Working Group Italian Society of Human Genetics(SIGU) Position Statement. Microarray application in prenatal diagnosis: a position statement from the working group on behalf of the Italian Society of Human Genetics (SIGU), November 2011. Ultrasound Obstet Gynecol 2012; in press, DOI: 10.1002/uog.11092.
    • (2012) Ultrasound Obstet Gynecol
    • Novelli, A.1    Grati, F.R.2    Ballarati, L.3
  • 7
    • 84863436203 scopus 로고    scopus 로고
    • 22q11.2 duplication, Available at: [accessed on 14 December 2011].
    • Firth HV. 22q11.2 duplication, 2009. Available at: [accessed on 14 December 2011].
    • (2009)
    • Firth, H.V.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.