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Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females.
Vacca M, Filippini F, Budillon A, Rossi V, Mercadante G, Manzati E, Gualandi F, Bigoni S, Trabanelli C, Pini G, Calzolari E, Ferlini A, Meloni I, Hayek G, Zappella M, Renieri A, D'Urso M, D'Esposito M, MacDonald F, Kerr A, Dhanjal S, Hultén M. Vacca M, et al. J Mol Med (Berl). 2001;78(11):648-55. doi: 10.1007/s001090000155. J Mol Med (Berl). 2001. PMID: 11269512
Dimensional phenotypic analysis and functional categorisation of mutations reveal novel genotype-phenotype associations in Rett syndrome.
Charman T, Neilson TC, Mash V, Archer H, Gardiner MT, Knudsen GP, McDonnell A, Perry J, Whatley SD, Bunyan DJ, Ravn K, Mount RH, Hastings RP, Hulten M, Orstavik KH, Reilly S, Cass H, Clarke A, Kerr AM, Bailey ME. Charman T, et al. Among authors: kerr am. Eur J Hum Genet. 2005 Oct;13(10):1121-30. doi: 10.1038/sj.ejhg.5201471. Eur J Hum Genet. 2005. PMID: 16077736
Review article: breaking new ground with Rett syndrome.
Kerr AM, Ravine D. Kerr AM, et al. J Intellect Disabil Res. 2003 Nov;47(Pt 8):580-7. doi: 10.1046/j.1365-2788.2003.00506.x. J Intellect Disabil Res. 2003. PMID: 14641805 Review. No abstract available.
Towards a full life with Rett disorder.
Kerr AM, Burford B. Kerr AM, et al. Pediatr Rehabil. 2001 Oct-Dec;4(4):157-68; discussion 155-6. doi: 10.1080/13638490210121694. Pediatr Rehabil. 2001. PMID: 12160356 Review.
Motion analysis of stereotyped hand movements in Rett syndrome.
Wright M, Van der Linden ML, Kerr AM, Burford B, Arrowsmith G, Middleton RL. Wright M, et al. Among authors: kerr am. J Intellect Disabil Res. 2003 Feb;47(Pt 2):85-9. doi: 10.1046/j.1365-2788.2003.00444.x. J Intellect Disabil Res. 2003. PMID: 12542573
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