Pathogenic copy number variations are associated with foetal short femur length in a tertiary referral centre study.

Cai, Meiying; Que, Yanting; Chen, Meihuan; Zhang, Min; Huang, Hailong; Xu, Liangpu; Lin, Na

Cai, Meiying; Que, Yanting; Chen, Meihuan; Zhang, Min; Huang, Hailong; Xu, Liangpu; Lin, Na.

Afiliação

Cai M; Medical Genetic Diagnosis and Therapy Center, Fujian Maternity and Child Health Hospital College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou, China.
Que Y; College of Clinical Medicine for Obstetrics and Gynecology and Pediatrics, Fujian Medical University, Fuzhou, China.
Chen M; Medical Genetic Diagnosis and Therapy Center, Fujian Maternity and Child Health Hospital College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou, China.
Zhang M; Medical Genetic Diagnosis and Therapy Center, Fujian Maternity and Child Health Hospital College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou, China.
Huang H; Medical Genetic Diagnosis and Therapy Center, Fujian Maternity and Child Health Hospital College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou, China.
Xu L; Medical Genetic Diagnosis and Therapy Center, Fujian Maternity and Child Health Hospital College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou, China.
Lin N; Medical Genetic Diagnosis and Therapy Center, Fujian Maternity and Child Health Hospital College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou, China.

J Cell Mol Med ; 27(16): 2354-2361, 2023 08.

Article em En | MEDLINE | ID: mdl-37401003

Assuntos

Variações do Número de Cópias de DNA; Feto; Gravidez; Feminino; Humanos; Variações do Número de Cópias de DNA/genética; Centros de Atenção Terciária; Idade Materna; Fêmur

Palavras-chave

7q11.23 microdeletion; chromosomal microarray analysis; copy number variation; fetal short femur; genetic abnormality; ultrasonography

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variações do Número de Cópias de DNA / Feto Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Pregnancy Idioma: En Revista: J Cell Mol Med Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China País de publicação: Reino Unido

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