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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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Dettagli Bibliografici
Pubblicato in:Balkan J Med Genet
Autori principali: Kocheva, SA, Martinova, K, Antevska-Trajkova, Z, Coneska-Jovanova, B, Eftimov, A, Dimovski, AJ
Natura: Artigo
Lingua:Inglês
Pubblicazione: De Gruyter 2016
Soggetti:
Accesso online: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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