Evaluation of chromosomal abnormalities and copy number variations in fetuses with ultrasonic soft markers.

Cai, Meiying; Lin, Na; Chen, Xuemei; Fu, Meimei; Guo, Nan; Xu, Liangpu; Huang, Hailong

Cai, Meiying; Lin, Na; Chen, Xuemei; Fu, Meimei; Guo, Nan; Xu, Liangpu; Huang, Hailong.

Afiliação

Cai M; Department of the Prenatal Diagnosis Center, Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou, China.
Lin N; Department of the Prenatal Diagnosis Center, Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou, China.
Chen X; Department of the Prenatal Diagnosis Center, Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou, China.
Fu M; Department of the Prenatal Diagnosis Center, Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou, China.
Guo N; Department of the Prenatal Diagnosis Center, Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou, China.
Xu L; Department of the Prenatal Diagnosis Center, Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou, China. xiliangpu@fjmu.edu.cn.
Huang H; Department of the Prenatal Diagnosis Center, Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou, China. huanghailong@fjmu.edu.cn.

BMC Med Genomics ; 14(1): 19, 2021 01 12.

Article em En | MEDLINE | ID: mdl-33435955

Assuntos

Diagnóstico Pré-Natal; Adulto; Aberrações Cromossômicas; Variações do Número de Cópias de DNA; Feminino; Humanos; Cariotipagem; Ultrassom

Palavras-chave

Copy number variations; Fetus; Single nucleotide polymorphism array analysis; Ultrasonic soft markers

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diagnóstico Pré-Natal Tipo de estudo: Diagnostic_studies Limite: Adult / Female / Humans Idioma: En Revista: BMC Med Genomics Assunto da revista: GENETICA MEDICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China País de publicação: Reino Unido

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