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

BACKGROUND: Some ultrasonic soft markers can be found during ultrasound examination. However, the etiology of the fetuses with ultrasonic soft markers is still unknown. This study aimed to evaluate the genetic etiology and clinical value of chromosomal abnormalities and copy number variations (CNVs)...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:BMC Med Genomics
Päätekijät: Cai, Meiying, Lin, Na, Chen, Xuemei, Fu, Meimei, Guo, Nan, Xu, Liangpu, Huang, Hailong
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2021
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7802188/
https://ncbi.nlm.nih.gov/pubmed/33435955
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-021-00870-w
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