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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Detalles Bibliográficos
Autores principales: Kocheva, SA, Martinova, K, Antevska-Trajkova, Z, Coneska-Jovanova, B, Eftimov, A, Dimovski, AJ
Formato: Online Artículo Texto
Lenguaje:English
Publicado: De Gruyter 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5026285/
https://www.ncbi.nlm.nih.gov/pubmed/27785413
http://dx.doi.org/10.1515/bjmg-2016-0012

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5026285/
https://www.ncbi.nlm.nih.gov/pubmed/27785413
http://dx.doi.org/10.1515/bjmg-2016-0012

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