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KBG syndrome
CLINICAL DESCRIPTION: KBG syndrome is characterized by macrodontia of upper central incisors, distinctive craniofacial features such as triangular face, prominent nasal bridge, thin upper lip and synophrys; skeletal findings including short stature, delayed bone age, and costovertebral anomalies; an...
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| Vydáno v: | Orphanet J Rare Dis |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5735576/ https://ncbi.nlm.nih.gov/pubmed/29258554 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-017-0736-8 |
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