The t(6;8)(q27;p11) translocation in a stem cell myeloproliferative disorder fuses a novel gene, FOP, to fibroblast growth factor receptor 1. [electronic resource]
Producer: 19990311Description: 1381-9 p. digitalISSN:- 0006-4971
- Adult
- Amino Acid Sequence
- Base Sequence
- Chromosomes, Human, Pair 6
- Chromosomes, Human, Pair 8
- Cloning, Molecular
- Genome, Human
- Hematopoietic Stem Cells -- pathology
- Humans
- Leucine -- genetics
- Male
- Molecular Sequence Data
- Myeloproliferative Disorders -- genetics
- Oncogene Proteins -- genetics
- Proto-Oncogene Proteins
- Receptors, Fibroblast Growth Factor -- genetics
- Translocation, Genetic
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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