Prenatal diagnosis of Pallister-Killian syndrome and literature review.

Wu, Xiaoqing; Xie, Xiaorui; Su, Linjuan; Lin, Na; Liang, Bin; Guo, Nan; Chen, Qingquan; Xu, Liangpu; Huang, Hailong

Wu, Xiaoqing; Xie, Xiaorui; Su, Linjuan; Lin, Na; Liang, Bin; Guo, Nan; Chen, Qingquan; Xu, Liangpu; Huang, Hailong.

Afiliação

Wu X; Fujian Provincial Key Laboratory for Prenatal Diagnosis and Birth Defect, Medical Genetic Diagnosis and Therapy Center of Fujian Provincial Maternity and Child Hospital, Affiliated Hospital of Fujian Medical University, Fuzhou, China.
Xie X; Department of Laboratory Medicine, Fujian Medical University, Fuzhou, China.
Su L; Fujian Provincial Key Laboratory for Prenatal Diagnosis and Birth Defect, Medical Genetic Diagnosis and Therapy Center of Fujian Provincial Maternity and Child Hospital, Affiliated Hospital of Fujian Medical University, Fuzhou, China.
Lin N; Fujian Provincial Key Laboratory for Prenatal Diagnosis and Birth Defect, Medical Genetic Diagnosis and Therapy Center of Fujian Provincial Maternity and Child Hospital, Affiliated Hospital of Fujian Medical University, Fuzhou, China.
Liang B; Fujian Provincial Key Laboratory for Prenatal Diagnosis and Birth Defect, Medical Genetic Diagnosis and Therapy Center of Fujian Provincial Maternity and Child Hospital, Affiliated Hospital of Fujian Medical University, Fuzhou, China.
Guo N; Fujian Provincial Key Laboratory for Prenatal Diagnosis and Birth Defect, Medical Genetic Diagnosis and Therapy Center of Fujian Provincial Maternity and Child Hospital, Affiliated Hospital of Fujian Medical University, Fuzhou, China.
Chen Q; Fujian Provincial Key Laboratory for Prenatal Diagnosis and Birth Defect, Medical Genetic Diagnosis and Therapy Center of Fujian Provincial Maternity and Child Hospital, Affiliated Hospital of Fujian Medical University, Fuzhou, China.
Xu L; Department of Laboratory Medicine, Fujian Medical University, Fuzhou, China.
Huang H; Fujian Provincial Key Laboratory for Prenatal Diagnosis and Birth Defect, Medical Genetic Diagnosis and Therapy Center of Fujian Provincial Maternity and Child Hospital, Affiliated Hospital of Fujian Medical University, Fuzhou, China.

J Cell Mol Med ; 25(18): 8929-8935, 2021 09.

Article em En | MEDLINE | ID: mdl-34405543

Assuntos

Transtornos Cromossômicos/diagnóstico; Feto/anormalidades; Cariotipagem/métodos; Diagnóstico Pré-Natal/métodos; Adulto; Cromossomos Humanos Par 12; Feminino; Humanos; Gravidez; Estudos Retrospectivos

Palavras-chave

Pallister-Killian syndrome; copy number variants sequencing; fluorescence in situ hybridization; nucleotide polymorphism array; prenatal diagnosis; ultrasound manifestation

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diagnóstico Pré-Natal / Transtornos Cromossômicos / Feto / Cariotipagem Tipo de estudo: Diagnostic_studies / Observational_studies / Risk_factors_studies Limite: Adult / Female / Humans / Pregnancy Idioma: En Ano de publicação: 2021 Tipo de documento: Article

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