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Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations
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發表在: | J Med Genet |
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Main Authors: | , , , , , , , , |
格式: | Artigo |
語言: | Inglês |
出版: |
2015
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主題: | |
在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4898782/ https://ncbi.nlm.nih.gov/pubmed/26671912 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmedgenet-2015-103476 |
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