Translocation breakpoints of chromosome 4 in male carriers: clinical features and implications for genetic counseling.

Zhang, H G; Wang, R X; Pan, Y; Zhu, J H; Xue, L T; Yang, X; Liu, R Z

Zhang, H G; Wang, R X; Pan, Y; Zhu, J H; Xue, L T; Yang, X; Liu, R Z.

Afiliación

Zhang HG; Center for Reproductive Medicine, Center for Prenatal Diagnosis, First Hospital, Jilin University, Changchun, Jilin, China.
Wang RX; Center for Reproductive Medicine, Center for Prenatal Diagnosis, First Hospital, Jilin University, Changchun, Jilin, China.
Pan Y; Center for Reproductive Medicine, Center for Prenatal Diagnosis, First Hospital, Jilin University, Changchun, Jilin, China.
Zhu JH; Center for Reproductive Medicine, Center for Prenatal Diagnosis, First Hospital, Jilin University, Changchun, Jilin, China.
Xue LT; Center for Reproductive Medicine, Center for Prenatal Diagnosis, First Hospital, Jilin University, Changchun, Jilin, China.
Yang X; Center for Reproductive Medicine, Center for Prenatal Diagnosis, First Hospital, Jilin University, Changchun, Jilin, China.
Liu RZ; Center for Reproductive Medicine, Center for Prenatal Diagnosis, First Hospital, Jilin University, Changchun, Jilin, China lrz410@126.com.

Genet Mol Res ; 15(4)2016 Dec 02.

Article en En | MEDLINE | ID: mdl-27966754

Asunto(s)

Aborto Espontáneo/genética; Azoospermia/genética; Puntos de Rotura del Cromosoma; Cromosomas Humanos Par 4/genética; Oligospermia/genética; Femenino; Asesoramiento Genético; Heterocigoto; Humanos; Masculino; Embarazo; Translocación Genética

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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Oligospermia / Cromosomas Humanos Par 4 / Aborto Espontáneo / Azoospermia / Puntos de Rotura del Cromosoma Tipo de estudio: Prognostic_studies Límite: Female / Humans / Male / Pregnancy Idioma: En Revista: Genet Mol Res Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA Año: 2016 Tipo del documento: Article País de afiliación: China

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