Prenatal detection of 10q22q23 duplications: dilemmas in phenotype prediction.

Kong, Grace Wing Shan; Cao, Ye; Huang, Jin; Cheng, Kwun Yue; Pursley, Amber Nolen; Rosenfeld, Jill Anne; Edwards, Janice G; Chan, Yiu Man; Cheung, Sau Wai; Leung, Tak Yeung; Choy, Kwong Wai

Kong, Grace Wing Shan; Cao, Ye; Huang, Jin; Cheng, Kwun Yue; Pursley, Amber Nolen; Rosenfeld, Jill Anne; Edwards, Janice G; Chan, Yiu Man; Cheung, Sau Wai; Leung, Tak Yeung; Choy, Kwong Wai.

Afiliação

Kong GW; Department of Obstetrics and Gynecology, The Chinese University of Hong Kong, Hong Kong.
Cao Y; Department of Obstetrics and Gynecology, The Chinese University of Hong Kong, Hong Kong.
Huang J; Shenzhen Research Institute, The Chinese University of Hong Kong, Shenzhen, China.
Cheng KY; Department of Obstetrics and Gynecology, The Chinese University of Hong Kong, Hong Kong.
Pursley AN; Department of Obstetrics and Gynecology, The Chinese University of Hong Kong, Hong Kong.
Rosenfeld JA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Edwards JG; Signature Genomic Laboratories, PerkinElmer, Inc., Spokane, WA, USA.
Chan YM; Genetic Counseling Program, University of South Carolina, Columbia, SC, USA.
Cheung SW; Department of Obstetrics and Gynecology, The Chinese University of Hong Kong, Hong Kong.
Leung TY; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Choy KW; Department of Obstetrics and Gynecology, The Chinese University of Hong Kong, Hong Kong.

Prenat Diagn ; 36(13): 1211-1216, 2016 Dec.

Article em En | MEDLINE | ID: mdl-27859473

Assuntos

Duplicação Cromossômica/genética; Cromossomos Humanos Par 10/genética; Fenótipo; Diagnóstico Pré-Natal/métodos; Anormalidades Congênitas/genética; Deficiências do Desenvolvimento/genética; Doenças em Gêmeos/genética; Feminino; Retardo do Crescimento Fetal/genética; Genótipo; Humanos; Hibridização in Situ Fluorescente; Análise em Microsséries; Medição da Translucência Nucal; Gravidez; Gravidez de Gêmeos/genética; Estudos Retrospectivos; Ultrassonografia Pré-Natal

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Diagnóstico Pré-Natal / Cromossomos Humanos Par 10 / Duplicação Cromossômica Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Pregnancy Idioma: En Ano de publicação: 2016 Tipo de documento: Article

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