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...
Main Authors: | , , , , , |
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Format: | Article |
Language: | English |
Published: |
Sciendo
2016-06-01
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Series: | Balkan Journal of Medical Genetics |
Subjects: | |
Online Access: | https://doi.org/10.1515/bjmg-2016-0012 |