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Dental management of a patient with 22q11.2 deletion syndrome (22q11.2DS)
22q11.2 deletion syndrome (22q11.2DS) is one of the most common microdeletion syndromes, with an incidence of approximately 1/2000–1/4000 live births; it is thought to be mainly attributable to a de novo deletion. The clinical phenotype of this syndrome is highly variable. Certain craniofacial and o...
Uloženo v:
| Vydáno v: | BMJ Case Rep |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BMJ Publishing Group
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6150132/ https://ncbi.nlm.nih.gov/pubmed/30232069 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2018-225765 |
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