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Rett syndrome: new clinical and molecular insights.
Williamson SL, Christodoulou J. Williamson SL, et al. Among authors: christodoulou j. Eur J Hum Genet. 2006 Aug;14(8):896-903. doi: 10.1038/sj.ejhg.5201580. Eur J Hum Genet. 2006. PMID: 16865103 Review.
Barth syndrome: clinical observations and genetic linkage studies.
Christodoulou J, McInnes RR, Jay V, Wilson G, Becker LE, Lehotay DC, Platt BA, Bridge PJ, Robinson BH, Clarke JT. Christodoulou J, et al. Am J Med Genet. 1994 Apr 15;50(3):255-64. doi: 10.1002/ajmg.1320500309. Am J Med Genet. 1994. PMID: 8042670
First prenatal diagnosis of the carnitine transporter defect.
Christodoulou J, Teo SH, Hammond J, Sim KG, Hsu BY, Stanley CA, Watson B, Lau KC, Wilcken B. Christodoulou J, et al. Am J Med Genet. 1996 Dec 2;66(1):21-4. doi: 10.1002/(SICI)1096-8628(19961202)66:1<21::AID-AJMG5>3.0.CO;2-Z. Am J Med Genet. 1996. PMID: 8957505
Diagnosis of Rett syndrome: can a radiograph help?
Glasson EJ, Bower C, Thomson MR, Fyfe S, Leonard S, Rousham E, Christodoulou J, Ellaway C, Leonard H. Glasson EJ, et al. Among authors: christodoulou j. Dev Med Child Neurol. 1998 Nov;40(11):737-42. doi: 10.1111/j.1469-8749.1998.tb12341.x. Dev Med Child Neurol. 1998. PMID: 9881802 Free article.
514 results