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A fetus with Kabuki syndrome 2 detected by chromosomal microarray analysis

Background: Kabuki syndrome is a rare multiple congenital anomaly syndrome characterized by distinct facial features, intellectual disability, cardiovascular and musculoskeletal abnormalities, persistence of fetal fingertip pads, and postnatal growth deficiency. Currently, the diagnosis mainly depen...

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Podrobná bibliografie
Vydáno v:Int J Clin Exp Pathol
Hlavní autoři: Lin, Chen-Zhao, Qi, Bi-Ru, Hu, Jian-Su, Huang, Xiu-Qiong
Médium: Artigo
Jazyk:Inglês
Vydáno: e-Century Publishing Corporation 2020
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7061791/
https://ncbi.nlm.nih.gov/pubmed/32211113
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