Endocrine profiling in patients with Fanconi anemia, homozygous for a FANCG founder mutation
Abstract Background Fanconi anemia (FA) is phenotypically diverse, hereditary condition associated with bone marrow failure, multiple physical abnormalities, and an increased susceptibility to the development of malignancies. Less recognized manifestations of FA include endocrine abnormalities. Inte...
Furkejuvvon:
| Váldodahkkit: | , , , , , , , |
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| Materiálatiipa: | Artigo |
| Giella: | Inglês |
| Almmustuhtton: |
Wiley
2020-08-01
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| Ráidu: | Molecular Genetics & Genomic Medicine |
| Fáttát: | |
| Liŋkkat: | https://doi.org/10.1002/mgg3.1351 |
| Fáddágilkorat: |
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