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The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies
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Development of an S-G2 micronucleus assay for the detection of in vitro chromosomal radiosensitivity in high-risk women subjected to early mammography screening for breast cancer
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Variant ataxia telangiectasia: clinical and molecular findings and evaluation of radiosensitive phenotypes in a patient and relatives
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X-linked sideroblastic anemia and ataxia: a new family with identification of a fourth ABCB7 gene mutation
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Steroids in intractable childhood epilepsy: clinical experience and review of the literature
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- Conference Paper
- C3
- open access
Differential organ involvement in peroxisomal disorders