Familial microdeletion 18p11.32 to 18p11.31 in a Chinese family with normal phenotype.

Han, Miaomiao; Wei, Lei; Liu, Fang; Gao, Xia

Han, Miaomiao; Wei, Lei; Liu, Fang; Gao, Xia.

Afiliación

Han M; Department of Obstetrics and Gynecology, Maternal and Child Health Hospital of Dongxihu District, Wuhan, Hubei, China.
Wei L; Department of Center for Reproductive Medicine, TaiHe Hospital, Hubei University of Medicine, Shiyan, Hubei, People's Republic of China.
Liu F; Department of Gynecology, Huangshi Love & Health Hospital Affiliated To Hubei Polytechnic University, Huangshi, Hubei, People's Republic of China.
Gao X; Department of Obstetrics, Renmin Hospital, Hubei University of Medicine, Shiyan, Hubei, People's Republic of China. gaoxiashiyan@yeah.com.

Mol Cytogenet ; 15(1): 12, 2022 Mar 24.

Article en En | MEDLINE | ID: mdl-35331298

Palabras clave

CMA; Microdeletion 18p11.32 to 18p11.31; Prenatal diagnosis; Unbalanced chromosome abnormality (UBCA)

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Mol Cytogenet Año: 2022 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido

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