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Germline but not Somatic De Novo Mutations Are Common in Human Congenital Diaphragmatic Hernia
BACKGROUND: Congenital diaphragmatic hernia (CDH) is a developmental defect of the diaphragm that causes high newborn morbidity and mortality. CDH is considered to be a multifactorial disease, with strong evidence implicating genetic factors. Although recent studies suggest the biological role of de...
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| Publicat a: | Birth Defects Res |
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| Autors principals: | , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5903934/ https://ncbi.nlm.nih.gov/pubmed/29570242 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/bdr2.1223 |
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