טוען...
Anatomic Malformations of the Middle and Inner Ear in 22q11.2 Deletion Syndrome: Case Series and Literature Review
BACKGROUND AND PURPOSE: The 22q11.2 deletion syndrome is characterized by a heterogenic phenotype, including hearing loss. The underlying cause of hearing loss, especially sensorineural hearing loss, is not yet clear. Therefore, our objective was to describe anatomic malformations in the middle and...
שמור ב:
| הוצא לאור ב: | AJNR Am J Neuroradiol |
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| Main Authors: | , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
American Society of Neuroradiology
2018
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7410659/ https://ncbi.nlm.nih.gov/pubmed/29545254 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3174/ajnr.A5588 |
| תגים: |
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