Pathogenic/likely pathogenic copy number variations and regions of homozygosity in fetal central nervous system malformations.

Zhi, Yunxiao; Liu, Ling; Cui, Shihong; Li, Ying; Chen, Xiaolin; Che, Jia; Han, Xiao; Zhao, Lanlan

Zhi, Yunxiao; Liu, Ling; Cui, Shihong; Li, Ying; Chen, Xiaolin; Che, Jia; Han, Xiao; Zhao, Lanlan.

Zhi Y; Department of the Third Hospital of Zhengzhou University, Zhengzhou, 450000, Henan, China.
Liu L; Department of the Third Hospital of Zhengzhou University, Zhengzhou, 450000, Henan, China.
Cui S; Department of the Third Hospital of Zhengzhou University, Zhengzhou, 450000, Henan, China. shihongcui@126.com.
Li Y; Department of the Third Hospital of Zhengzhou University, Zhengzhou, 450000, Henan, China.
Chen X; Department of the Third Hospital of Zhengzhou University, Zhengzhou, 450000, Henan, China.
Che J; Department of the Third Hospital of Zhengzhou University, Zhengzhou, 450000, Henan, China.
Han X; Department of the Third Hospital of Zhengzhou University, Zhengzhou, 450000, Henan, China.
Zhao L; Department of the Third Hospital of Zhengzhou University, Zhengzhou, 450000, Henan, China.

Arch Gynecol Obstet ; 308(6): 1723-1735, 2023 12.

Article en En | MEDLINE | ID: mdl-36464758

Asunto(s)

Enfermedades del Sistema Nervioso Central; Malformaciones del Sistema Nervioso; Embarazo; Femenino; Humanos; Variaciones en el Número de Copia de ADN; Estudios Retrospectivos; Feto; Malformaciones del Sistema Nervioso/diagnóstico por imagen; Malformaciones del Sistema Nervioso/genética; Análisis por Micromatrices; Diagnóstico Prenatal; Aberraciones Cromosómicas

Palabras clave

Abnormality; Central nervous system; Fetus; P/LP CNVs; ROH; SNP array

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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades del Sistema Nervioso Central / Malformaciones del Sistema Nervioso Límite: Female / Humans / Pregnancy Idioma: En Año: 2023 Tipo del documento: Article

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