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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...
Uloženo v:
| Vydáno v: | Int J Clin Exp Pathol |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
e-Century Publishing Corporation
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7061791/ https://ncbi.nlm.nih.gov/pubmed/32211113 |
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