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Volumn 114, Issue 5, 2009, Pages 1161-1163

Array comparative genomic hybridization in prenatal diagnosis
[No Author Info available]

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME NUMBER; CHROMOSOME REARRANGEMENT; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL DISORDER; COST BENEFIT ANALYSIS; CYTOGENETICS; DEVELOPMENTAL DISORDER; INTERMETHOD COMPARISON; KARYOTYPING; MENTAL DEFICIENCY; NOTE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; ARTICLE; CHROMOSOME ABERRATION; DNA MICROARRAY; ECONOMICS; FEMALE; HUMAN; METHODOLOGY; PREGNANCY;

EID: 73549121749     PISSN: 00297844     EISSN: None     Source Type: Journal    
DOI: 10.1097/AOG.0b013e3181c33cad     Document Type: Note
Times cited : (121)

References (11)
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    • DOI 10.1086/421250
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    • Schaeffer, A.J.1    Chung, J.2    Heretis, K.3    Wong, A.4    Ledbetter, D.H.5    Martin, C.L.6
  • 5
    • 34249680839 scopus 로고    scopus 로고
    • Use of array CGH in the evaluation of dysmorphology, malformations, developmental delay, and idiopathic mental retardation
    • DOI 10.1016/j.gde.2007.04.009, PII S0959437X07000743
    • Stankiewicz P, Beaudet AL. Use of array CGH in the evaluation of dysmorphology, malformations, developmental delay, and idiopathic mental retardation. Curr Opin Genet Dev 2007;17:182-192 (Pubitemid 46843553)
    • (2007) Current Opinion in Genetics and Development , vol.17 , Issue.3 , pp. 182-192
    • Stankiewicz, P.1    Beaudet, A.L.2
  • 6
    • 33751172713 scopus 로고    scopus 로고
    • Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization
    • Sahoo T, Cheung SW, Ward P, Darilek S, Patel A, del Gaudio D, et al. Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization. Genet Med 2006;8:719-727
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    • Sahoo, T.1    Cheung, S.W.2    Ward, P.3    Darilek, S.4    Patel, A.5    Del Gaudio, D.6
  • 7
    • 54049094444 scopus 로고    scopus 로고
    • Recurrent rearrangements of chromosome lq21.1 and variable pediatric phenotypes
    • Mefford HC, Sharp AJ, Baker C, Itsara A, Jiang Z, Buysse K, et al. Recurrent rearrangements of chromosome lq21.1 and variable pediatric phenotypes. N Engl J Med 2008;359: 1685-1699
    • (2008) N Engl J Med , vol.359 , pp. 1685-1699
    • Mefford, H.C.1    Sharp, A.J.2    Baker, C.3    Itsara, A.4    Jiang, Z.5    Buysse, K.6
  • 8
    • 44249121777 scopus 로고    scopus 로고
    • Novel microdeletion syndromes detected by chromosome microarrays
    • Slavotinek AM. Novel microdeletion syndromes detected by chromosome microarrays. Hum Genet 2008;124:1-17.
    • (2008) Hum Genet , vol.124 , pp. 1-17
    • Slavotinek, A.M.1
  • 9
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    • A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism
    • Koolen DA, Vissers LE, Pfundt R, de Leeuw N, Knight SJ, Regan R, et al. A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism. Nat Genet 2006;38:999-1001.
    • (2006) Nat Genet , vol.38 , pp. 999-1001
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  • 11


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.