Prenatal diagnosis of a 4.5-Mb deletion at chromosome 4q35.1q35.2: Case report and literature review

OBJECTIVE: We present a genetic analysis of an asymptomatic family with a 4q terminal deletion; we also review other similar published studies and discuss the genotype–phenotype correlation. METHODS: A karyotype analysis was performed on the amniotic fluid cells of a woman at 24 weeks of pregnancy a...

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Detalles Bibliográficos
Autores principales: Xiao, Gefei, Qiu, Xianrong, Zhou, Yuqiu, Tan, Gongjun, Shen, Yao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8600819/
https://www.ncbi.nlm.nih.gov/pubmed/34794455
http://dx.doi.org/10.1186/s13039-021-00573-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8600819/
https://www.ncbi.nlm.nih.gov/pubmed/34794455
http://dx.doi.org/10.1186/s13039-021-00573-y

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