Association between clinical variations and copy number variations in cases with Turner syndrome.

Aksoy, Ezgi; Cogulu, Ozgur; Pariltay, Erhan; Ozen, Samim; Ata, Aysun; Karaca, Emin; Darcan, Sukran

Aksoy, Ezgi; Cogulu, Ozgur; Pariltay, Erhan; Ozen, Samim; Ata, Aysun; Karaca, Emin; Darcan, Sukran.

Afiliação

Aksoy E; Department of Child Health and Diseases, Faculty of Medicine, Ege University, Izmir, Turkey.
Cogulu O; Department of Medical Genetics, Faculty of Medicine, Ege University, Izmir, Turkey.
Pariltay E; Department of Medical Genetics, Faculty of Medicine, Ege University, Izmir, Turkey.
Ozen S; Department of Pediatric Endocrinology and Diabetes, Faculty of Medicine, Ege University, Izmir, Turkey.
Ata A; Department of Pediatric Endocrinology and Diabetes, Faculty of Medicine, Ege University, Izmir, Turkey.
Karaca E; Department of Medical Genetics, Faculty of Medicine, Ege University, Izmir, Turkey.
Darcan S; Department of Pediatric Endocrinology and Diabetes, Faculty of Medicine, Ege University, Izmir, Turkey.

J Pediatr Endocrinol Metab ; 35(9): 1161-1168, 2022 Sep 27.

Article em En | MEDLINE | ID: mdl-35953302

Assuntos

Síndrome de Turner; Adolescente; Criança; Pré-Escolar; Variações do Número de Cópias de DNA/genética; Hormônio Foliculoestimulante; Humanos; Lactente; Recém-Nascido; Cariótipo; Cariotipagem; Síndrome de Turner/diagnóstico; Síndrome de Turner/genética

Palavras-chave

Turner syndrome; clinical variations; copy number variations; microarray

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Turner Tipo de estudo: Diagnostic_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Humans / Infant / Newborn Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google