Prenatal diagnosis of trisomy 6q25.3-qter and monosomy 10q26.12-qter by array CGH in a fetus with an apparently normal karyotype.

Marinescu, Ponnila S; Saller, Devereux N; Parks, W Tony; Yatsenko, Svetlana A; Rajkovic, Aleksandar

Marinescu, Ponnila S; Saller, Devereux N; Parks, W Tony; Yatsenko, Svetlana A; Rajkovic, Aleksandar.

Afiliação

Marinescu PS; Department of Obstetrics and Gynecology, University of Virginia Health System Charlottesville, Virginia.
Saller DN; Division of Medical Genetics, Department of Obstetrics, Gynecology and Reproductive Sciences, Magee-Womens Hospital of University of Pittsburgh Medical Center Pittsburgh, Pennsylvania.
Parks WT; Department of Pathology, University of Pittsburgh School of Medicine Pittsburgh, Pennsylvania.
Yatsenko SA; Division of Medical Genetics, Department of Obstetrics, Gynecology and Reproductive Sciences, Magee-Womens Hospital of University of Pittsburgh Medical Center Pittsburgh, Pennsylvania ; Department of Pathology, University of Pittsburgh School of Medicine Pittsburgh, Pennsylvania.
Rajkovic A; Division of Medical Genetics, Department of Obstetrics, Gynecology and Reproductive Sciences, Magee-Womens Hospital of University of Pittsburgh Medical Center Pittsburgh, Pennsylvania ; Department of Pathology, University of Pittsburgh School of Medicine Pittsburgh, Pennsylvania ; Department of Huma

Clin Case Rep ; 3(2): 92-5, 2015 Feb.

Article em En | MEDLINE | ID: mdl-25767704

Palavras-chave

Array CGH; deletion 10q; duplication 6q; fetal ultrasound; prenatal diagnosis; unbalanced translocation

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Clin Case Rep Ano de publicação: 2015 Tipo de documento: Article

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google