[Clinical and genetic characteristic in patients with disorders of sex development caused by Y chromosome copy number variant].

Xia, J K; Tian, F Y; Hou, Y Q; Zhao, Y J; Kong, X D

Xia, J K; Tian, F Y; Hou, Y Q; Zhao, Y J; Kong, X D.

Afiliação

Xia JK; Prenatal and Genetic Diagnosis Center, Department of Gynaecology and Obstetrics, the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
Tian FY; Department of Pediatrics, the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
Hou YQ; Prenatal and Genetic Diagnosis Center, Department of Gynaecology and Obstetrics, the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
Zhao YJ; Prenatal and Genetic Diagnosis Center, Department of Gynaecology and Obstetrics, the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
Kong XD; Prenatal and Genetic Diagnosis Center, Department of Gynaecology and Obstetrics, the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.

Zhonghua Er Ke Za Zhi ; 61(5): 459-463, 2023 May 02.

Article em Zh | MEDLINE | ID: mdl-37096267

Assuntos

Variações do Número de Cópias de DNA; Síndrome de Turner; Humanos; Feminino; Hibridização in Situ Fluorescente; Estudos Retrospectivos; Cromossomos Humanos Y

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Turner / Variações do Número de Cópias de DNA Tipo de estudo: Observational_studies / Prognostic_studies Limite: Female / Humans Idioma: Zh Revista: Zhonghua Er Ke Za Zhi Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China

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