[Identification of a de novo interstitial 21q22.12q22.13 deletion in a patient with intellectual disability].

Peng, Ying; Jia, ZhengJun; Pang, Jialun; Hu, Jiancheng; Xi, Hui; Wang, Hua

Peng, Ying; Jia, ZhengJun; Pang, Jialun; Hu, Jiancheng; Xi, Hui; Wang, Hua.

Affiliation

Peng Y; Prenatal Diagnosis Center of Hunan Province, Maternal and Child Health Care Hospital of Hunan Province, Changsha, Hunan 410008, China. wanghua213@aliyun.com.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi ; 36(7): 704-707, 2019 Jul 10.

Article in Zh | MEDLINE | ID: mdl-31302916

Subject(s)

Developmental Disabilities/genetics; Epilepsy/genetics; Intellectual Disability/genetics; Protein Serine-Threonine Kinases/genetics; Protein-Tyrosine Kinases/genetics; Sequence Deletion; Child; Genetic Association Studies; Humans; Karyotyping; Dyrk Kinases

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Protein-Tyrosine Kinases / Developmental Disabilities / Sequence Deletion / Protein Serine-Threonine Kinases / Epilepsy / Intellectual Disability Type of study: Diagnostic_studies Limits: Child / Humans Language: Zh Journal: Zhonghua Yi Xue Yi Chuan Xue Za Zhi Journal subject: GENETICA MEDICA Year: 2019 Type: Article Affiliation country: China

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