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| Title | Author/Creator | Date | Full Text | Reviewed | |
|---|---|---|---|---|---|
| Association of paediatric mastocytosis with a polymorphism resulting in an amino acid substitution (M541L) in the transmembrane domain of c-KIT | Foster, R.; Byrnes, E.; Ashman, L. K.; Meldrum, C.; Griffith, R.... More | 2008 | — | 
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| A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology | Talseth-Palmer, B. A.; Bowden, N. A.; Scott, R. J.; Meldrum, C.; Nicholl, J.... More | 2009 | — |
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Author/Creator
- Ashman, L. K. (1)
- Bowden, N. A. (1)
- Bratkovic, D. (1)
- Braue, A. (1)
- Byrnes, E. (1)
- Ferrao, P. (1)
- Foster, R. (1)
- Friend, K. (1)
- Griffith, R. (1)
Keyword
- SNP arrays (1)
- chromosome 2 (1)
- cutaneous mastocytosis (1)
- cytogenetic (1)
- proto-oncogene protein c-Kit (1)
