Cargando…
Clinical, cytogenetic, and molecular findings in a fetus with ultrasonic multiple malformations, 4q duplication, and 7q deletion: A case report and literature review
RATIONALE: Chromosome deletion/duplication has been reported to be associated with mental disability and dysmorphism according to the accumulated research evidence. PATIENT CONCERNS: A 25-year-old woman underwent amniocentesis for cytogenetic and single-nucleotide polymorphism (SNP) array analysis a...
Autores principales: | Yue, Fagui, Jiang, Yuting, Yu, Yang, Yang, Xiao, Zhang, Hongguo, Liu, Ruizhi, Wang, Ruixue |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6250448/ https://www.ncbi.nlm.nih.gov/pubmed/30407316 http://dx.doi.org/10.1097/MD.0000000000013094 |
Ejemplares similares
-
Prenatal phenotypes and pregnancy outcomes of fetuses with recurrent 1q21.1 microdeletions and microduplications
por: Yue, Fagui, et al.
Publicado: (2023) -
Prenatal diagnosis of a de novo 15q11.2 microdeletion in a maternal inv(4)(p15q31) fetus with increased nuchal translucency: A case report and literature review
por: Sun, Meiling, et al.
Publicado: (2020) -
Prenatal detection of distal 1q21.1q21.2 microduplication with abnormal ultrasound findings: Two cases report and literature review
por: Zhang, Hongguo, et al.
Publicado: (2021) -
Prenatal detection of a 3q29 microdeletion in a fetus with ventricular septum defect: A case report and literature review
por: Yue, Fagui, et al.
Publicado: (2021) -
Molecular cytogenetic characterization of partial monosomy 2p and trisomy 16q in a newborn: A case report
por: Yue, Fagui, et al.
Publicado: (2019)