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| Title | Author/Creator | Date | Full Text | Reviewed | |
|---|---|---|---|---|---|
| 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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| Twenty-six novel EFNB1 mutations in familial and sporadic cranlofrontonasal syndrome (CFNS) | Wieland, I.; Reardon, W.; Jakubiczka, S.; Franco, B.; Kress, W.... More | 2005 | — |
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Author/Creator
- Bowden, N. A. (1)
- Bratkovic, D. (1)
- Edwards, Matthew (1)
- Franco, B. (1)
- Friend, K. (1)
- Haan, E. (1)
- Jakubiczka, S. (1)
- Konig, R. (1)
- Kress, W. (1)
Keyword
- CFND (1)
- CFNS (1)
- EFNB1 (1)
- SNP arrays (1)
- X-linked (1)
- abnormalities (1)
- cause craniofrontonasal syndrome (1)
- chromosome 2 (1)
- cytogenetic (1)
- dysplasia (1)
