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Hallermann-Streiff Syndrome: No Evidence for a Link to Laminopathies
Hallermann-Streiff syndrome (HSS) is a rare inherited disorder characterized by malformations of the cranium and facial bones, congenital cataracts, microphthalmia, skin atrophy, hypotrichosis, proportionate short stature, teeth abnormalities, and a typical facial appearance with prominent forehead,...
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| Main Authors: | , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
S. Karger AG
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3343748/ https://ncbi.nlm.nih.gov/pubmed/22570643 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000334317 |
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