Prenatal detection of a 3q29 microdeletion in a fetus with ventricular septum defect: A case report and literature review

RATIONALE: Chromosomal 3q deletion is a recurrent genomic alternation, which is rarely reported in clinic. PATIENT CONCERNS: A 27-year-old woman underwent amniocentesis for cytogenetic analysis and single nucleotide polymorphism (SNP) array analysis at 27 weeks of gestation, due to ventricular septu...

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Detalles Bibliográficos
Autores principales: Yue, Fagui, Deng, Shu, Xi, Qi, Jiang, Yuting, He, Jing, Zhang, Hongguo, Liu, Ruizhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
3500
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7793333/
https://www.ncbi.nlm.nih.gov/pubmed/33429816
http://dx.doi.org/10.1097/MD.0000000000024224

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7793333/
https://www.ncbi.nlm.nih.gov/pubmed/33429816
http://dx.doi.org/10.1097/MD.0000000000024224

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