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...
Sábháilte in:
| Príomhchruthaitheoirí: | , , , , , |
|---|---|
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe / Cruthaithe: |
Sciendo
2016-06-01
|
| Sraith: | Balkan Journal of Medical Genetics |
| Ábhair: | |
| Rochtain ar líne: | https://doi.org/10.1515/bjmg-2016-0012 |
| Clibeanna: |
Níl clibeanna ann, Bí ar an gcéad duine le clib a chur leis an taifead seo!
|