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Noonan syndrome and clinically related disorders
Noonan syndrome is a relatively common, clinically variable developmental disorder. Cardinal features include postnatally reduced growth, distinctive facial dysmorphism, congenital heart defects and hypertrophic cardiomyopathy, variable cognitive deficit and skeletal, ectodermal and hematologic anom...
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| Main Authors: | , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
2011
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3058199/ https://ncbi.nlm.nih.gov/pubmed/21396583 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.beem.2010.09.002 |
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