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Evaluation of clinical diagnostic criteria for neurofibromatosis 2.
Baser ME, Friedman JM, Wallace AJ, Ramsden RT, Joe H, Evans DG. Baser ME, et al. Among authors: evans dg. Neurology. 2002 Dec 10;59(11):1759-65. doi: 10.1212/01.wnl.0000035638.74084.f4. Neurology. 2002. PMID: 12473765 Clinical Trial.
The location of constitutional neurofibromatosis 2 (NF2) splice site mutations is associated with the severity of NF2.
Baser ME, Kuramoto L, Woods R, Joe H, Friedman JM, Wallace AJ, Ramsden RT, Olschwang S, Bijlsma E, Kalamarides M, Papi L, Kato R, Carroll J, Lázaro C, Joncourt F, Parry DM, Rouleau GA, Evans DG. Baser ME, et al. Among authors: evans dg. J Med Genet. 2005 Jul;42(7):540-6. doi: 10.1136/jmg.2004.029504. J Med Genet. 2005. PMID: 15994874 Free PMC article. Review.
Genotype-phenotype correlations for cataracts in neurofibromatosis 2.
Baser ME, Kuramoto L, Joe H, Friedman JM, Wallace AJ, Ramsden RT, Evans DG. Baser ME, et al. Among authors: evans dg. J Med Genet. 2003 Oct;40(10):758-60. doi: 10.1136/jmg.40.10.758. J Med Genet. 2003. PMID: 14569124 Free PMC article. No abstract available.
Constitutional rearrangements of chromosome 22 as a cause of neurofibromatosis 2.
Tsilchorozidou T, Menko FH, Lalloo F, Kidd A, De Silva R, Thomas H, Smith P, Malcolmson A, Dore J, Madan K, Brown A, Yovos JG, Tsaligopoulos M, Vogiatzis N, Baser ME, Wallace AJ, Evans DG. Tsilchorozidou T, et al. Among authors: evans dg. J Med Genet. 2004 Jul;41(7):529-34. doi: 10.1136/jmg.2003.016774. J Med Genet. 2004. PMID: 15235024 Free PMC article. Review. No abstract available.
1,362 results