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| Title | Author/Creator | Date | Full Text | Reviewed | |
|---|---|---|---|---|---|
| Identification and characterization of two novel JARID1C mutations: suggestion of an emerging genotype-phenotype correlation | Rujirabanjerd, Sinitdhorn; Nelson, John; Futreal, P. Andrew; Stratton, Michael R.; Gecz, Jozef... More | 2010 | — | 
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| A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation | Tarpey, Patrick S.; Smith, Raffaella; Stephens, Phil; Blow, Matt; Greenman, Chris... More | 2009 | — |
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Author/Creator
- Andrews, Jenny (1)
- Barthorpe, Syd (1)
- Blow, Matt (1)
- Buck, Gemma (1)
- Dicks, Ed (1)
- Futreal, P. Andrew (1)
- Gecz, Jozef (1)
Keyword
- JARID1C (1)
- JmjC domain (1)
- X-chromosome coding (1)
- X-linked mental retardation (1)
- disease-causing mutations (1)
- mental retardation (1)
- mutation analysis (1)
- resequencing (1)
