[Prenatal diagnosis of partial deletion of NRXN1 gene with combined CNV-seq and qPCR assays].

Wang, Lixia; Shi, Panlai; Ren, Hua'nan; Xue, Shuyuan; Kong, Xiangdong

Wang, Lixia; Shi, Panlai; Ren, Hua'nan; Xue, Shuyuan; Kong, Xiangdong.

Affiliation

Wang L; Prenatal Diagnosis Center, Urumqi Maternal and Child Health Care Hospital, Urumqi, Xinjiang 830000, China. kongxd@263.net.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi ; 39(11): 1200-1204, 2022 Nov 10.

Article in Zh | MEDLINE | ID: mdl-36317203

Subject(s)

Cell Adhesion Molecules, Neuronal; DNA Copy Number Variations; Female; Humans; Pregnancy; Calcium-Binding Proteins/genetics; Cell Adhesion Molecules, Neuronal/genetics; Nerve Tissue Proteins/genetics; Neural Cell Adhesion Molecules/genetics; Prenatal Diagnosis; Real-Time Polymerase Chain Reaction; Infant, Newborn

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Full text: 1 Database: MEDLINE Main subject: Cell Adhesion Molecules, Neuronal / DNA Copy Number Variations Type of study: Diagnostic_studies / Guideline / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Newborn / Pregnancy Language: Zh Journal: Zhonghua Yi Xue Yi Chuan Xue Za Zhi Journal subject: GENETICA MEDICA Year: 2022 Type: Article Affiliation country: China

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