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22q11.2 microdeletion in two adolescent patients who presented with convulsion
22q11.2 microdeletion which involves DiGeorge syndrome, velo-cardiofacial syndrome and conotruncal anomaly face syndrome occurs as a result of a deletion in the short segment of the long arm of the 22th chromosome. Patients with this syndrome have a wide clinical spectrum including learning difficul...
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| Publicado en: | Turk Pediatri Ars |
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| Autores principales: | , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Turkish Pediatrics Association
2014
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4462263/ https://ncbi.nlm.nih.gov/pubmed/26078635 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5152/tpa.2014.658 |
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