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NTNG1 mutations are a rare cause of Rett syndrome. [electronic resource] by
- Archer, Hayley L
- Evans, Julie C
- Millar, David S
- Thompson, Peter W
- Kerr, Alison M
- Leonard, Helen
- Christodoulou, John
- Ravine, David
- Lazarou, Lazarus
- Grove, Lucy
- Verity, Christopher
- Whatley, Sharon D
- Pilz, Daniela T
- Sampson, Julian R
- Clarke, Angus J
Producer: 20060530
In:
American journal of medical genetics. Part A vol. 140
Availability: No items available.
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Dimensional phenotypic analysis and functional categorisation of mutations reveal novel genotype-phenotype associations in Rett syndrome. [electronic resource] by
- Charman, Tony
- Neilson, Tracey C S
- Mash, Veronica
- Archer, Hayley
- Gardiner, Mary T
- Knudsen, Gun P S
- McDonnell, Aoibhinn
- Perry, Jacqueline
- Whatley, Sharon D
- Bunyan, David J
- Ravn, Kirstine
- Mount, Rebecca H
- Hastings, Richard P
- Hulten, Maj
- Orstavik, Karen Helene
- Reilly, Sheena
- Cass, Hilary
- Clarke, Angus
- Kerr, Alison M
- Bailey, Mark E S
Producer: 20051108
In:
European journal of human genetics : EJHG vol. 13
Availability: No items available.
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