[Genetic screening and prenatal diagnosis for high risk families of Fragile X syndrome].

Xi, Hui; Zhang, Yanan; Qin, Liyan; Kang, Huaixing; Duan, Ranhui; Jia, Zhengjun; Wang, Hua

Xi, Hui; Zhang, Yanan; Qin, Liyan; Kang, Huaixing; Duan, Ranhui; Jia, Zhengjun; Wang, Hua.

Affiliation

Xi H; Center of Hunan Provincial Prenatal Diagnosis, Hunan Maternal and Child Health Hospital, Changsha, Hunan 410008, China. wanghua213@aliyun.com.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi ; 35(5): 653-656, 2018 Oct 10.

Article in Zh | MEDLINE | ID: mdl-30298488

Subject(s)

Fetal Diseases/diagnosis; Fragile X Syndrome/embryology; Fragile X Syndrome/genetics; Adult; Alleles; Female; Fetal Diseases/genetics; Fragile X Mental Retardation Protein; Fragile X Syndrome/complications; Fragile X Syndrome/psychology; Genetic Testing; Humans; Intellectual Disability/etiology; Male; Mutation; Pedigree; Pregnancy; Prenatal Diagnosis; Young Adult

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Full text: 1 Database: MEDLINE Main subject: Fetal Diseases / Fragile X Syndrome Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limits: Adult / Female / Humans / Male / Pregnancy Language: Zh Journal: Zhonghua Yi Xue Yi Chuan Xue Za Zhi Journal subject: GENETICA MEDICA Year: 2018 Type: Article Affiliation country: China

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