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18q deletion in a cystic fibrosis infant, increased morbidity and challenge for correct treatment choices: a case report
Cystic Fibrosis (CF) is the most frequent recessive disease of Caucasian patients. Association with other diseases or syndromes has previously been reported. Co-morbidity may be a challenge for clinicians, who have to face more severe problems. We have described a CF infant, F508del homozygote, diag...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3120749/ https://ncbi.nlm.nih.gov/pubmed/21586141 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1824-7288-37-22 |
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