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T-lymphoblastic leukemia/lymphoma in macedonian patients with Nijmegen breakage syndrome
Nijmegen breakage syndrome (NBS) is a rare autosomal recessive chromosomal instability disorder characterized by microcephaly, immunodeficiency, radiosensitivity and a very high predisposition to malignancy. The gene responsible for the disease, NBS1, is located on chromosome 8q21 and encodes a prot...
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| Publicado en: | Balkan J Med Genet |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
De Gruyter
2016
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5026285/ https://ncbi.nlm.nih.gov/pubmed/27785413 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1515/bjmg-2016-0012 |
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