PHF6 mutations in paediatric acute myeloid leukaemia
Language English Country England, Great Britain Media print-electronic
Document type Letter, Research Support, Non-U.S. Gov't
PubMed
27885656
DOI
10.1111/bjh.13891
Knihovny.cz E-resources
- Keywords
- PHF6, cytogenetics, mutation analysis, myeloid leukaemia, paediatric oncology,
- MeSH
- Leukemia, Myeloid, Acute genetics MeSH
- Child MeSH
- Infant MeSH
- Humans MeSH
- Adolescent MeSH
- Mutation MeSH
- Infant, Newborn MeSH
- Child, Preschool MeSH
- Repressor Proteins MeSH
- Carrier Proteins genetics MeSH
- Check Tag
- Child MeSH
- Infant MeSH
- Humans MeSH
- Adolescent MeSH
- Male MeSH
- Infant, Newborn MeSH
- Child, Preschool MeSH
- Female MeSH
- Publication type
- Letter MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- PHF6 protein, human MeSH Browser
- Repressor Proteins MeSH
- Carrier Proteins MeSH
AML BFM Study Group Paediatric Haematology Oncology Universitätsklinikum Essen Essen Germany
Dutch Childhood Oncology Group The Hague the Netherlands
Haematology Hôpital Saint Louis Paris France
Paediatric Haematology Oncology 2nd Medical School Charles University Prague Czech Republic
Paediatric Oncology Haematology Erasmus MC Sophia Children's Hospital Rotterdam the Netherlands
Princess Máxima Centre for Paediatric Oncology Utrecht the Netherlands
References provided by Crossref.org
