Validation of a Chromosomal Microarray for Prenatal Diagnosis Using a Prospective Cohort of Pregnancies with Increased Risk for Chromosome Abnormalities.

Wright, Dale; Carey, Louise; Battersby, Siobhan; Nguyen, Thuy; Clarke, Melanie; Nash, Benjamin; Gulesserian, Elee; Cross, Jill; Darmanian, Artur

Wright, Dale; Carey, Louise; Battersby, Siobhan; Nguyen, Thuy; Clarke, Melanie; Nash, Benjamin; Gulesserian, Elee; Cross, Jill; Darmanian, Artur.

Afiliação

Wright D; Department of Cytogenetics, Sydney Genome Diagnostics, The Children's Hospital at Westmead , Westmead, Australia .
Carey L; Department of Cytogenetics, Sydney Genome Diagnostics, The Children's Hospital at Westmead , Westmead, Australia .
Battersby S; Department of Cytogenetics, Sydney Genome Diagnostics, The Children's Hospital at Westmead , Westmead, Australia .
Nguyen T; Department of Cytogenetics, Sydney Genome Diagnostics, The Children's Hospital at Westmead , Westmead, Australia .
Clarke M; Department of Cytogenetics, Sydney Genome Diagnostics, The Children's Hospital at Westmead , Westmead, Australia .
Nash B; Department of Cytogenetics, Sydney Genome Diagnostics, The Children's Hospital at Westmead , Westmead, Australia .
Gulesserian E; Department of Cytogenetics, Sydney Genome Diagnostics, The Children's Hospital at Westmead , Westmead, Australia .
Cross J; Department of Cytogenetics, Sydney Genome Diagnostics, The Children's Hospital at Westmead , Westmead, Australia .
Darmanian A; Department of Cytogenetics, Sydney Genome Diagnostics, The Children's Hospital at Westmead , Westmead, Australia .

Genet Test Mol Biomarkers ; 20(12): 791-798, 2016 Dec.

Article em En | MEDLINE | ID: mdl-27690282

Assuntos

Transtornos Cromossômicos/diagnóstico; Hibridização Genômica Comparativa/métodos; Complicações na Gravidez/genética; Diagnóstico Pré-Natal/métodos; Aneuploidia; Transtornos Cromossômicos/genética; Síndrome de Down/diagnóstico; Feminino; Humanos; Cariótipo; Cariotipagem/métodos; Mosaicismo; Análise de Sequência com Séries de Oligonucleotídeos/métodos; Gravidez; Estudos Prospectivos; Fatores de Risco; Sensibilidade e Especificidade; Trissomia/diagnóstico

Palavras-chave

chromosome microarray; copy number abnormality; prenatal diagnosis

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Complicações na Gravidez / Diagnóstico Pré-Natal / Transtornos Cromossômicos / Hibridização Genômica Comparativa Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Risk_factors_studies Limite: Female / Humans / Pregnancy Idioma: En Ano de publicação: 2016 Tipo de documento: Article

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