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Bardet-Biedl Syndrome 3 regulates development of cranial base midline structures
Bardet-Biedl Syndrome (BBS) is an autosomal recessive disorder and is classified as one of the ciliopathy. The patients manifest a characteristic craniofacial dysmorphology but the effects of Bbs3 deficiency in the developmental process during the craniofacial pathogenesis are still incompletely und...
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| Publicado no: | Bone |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5519131/ https://ncbi.nlm.nih.gov/pubmed/27170093 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bone.2016.02.017 |
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