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Fetal chondrodysplasia punctata associated with maternal autoimmune diseases: a review
Chondrodysplasia punctata (CDP) is a skeletal abnormality characterized by premature calcification that is usually noticeable in the prenatal period and infancy. Etiologically, the condition is heterogeneous, and the causes include fetal conditions such as chromosome abnormalities, peroxisomal disor...
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| Vydáno v: | Appl Clin Genet |
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| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Dove Medical Press
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5918624/ https://ncbi.nlm.nih.gov/pubmed/29720879 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/TACG.S150982 |
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