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Page 1
Expanding phenotype of XNP mutations: mild to moderate mental retardation.
Yntema HG, Poppelaars FA, Derksen E, Oudakker AR, van Roosmalen T, Jacobs A, Obbema H, Brunner HG, Hamel BC, van Bokhoven H. Yntema HG, et al. Among authors: van roosmalen t. Am J Med Genet. 2002 Jul 1;110(3):243-7. doi: 10.1002/ajmg.10446. Am J Med Genet. 2002. PMID: 12116232
Psychometric assessment of families with X-linked mental retardation.
van Roosmalen T, Smits AP, Thoonen GH, Hamel BC, Assman-Hulmans CF, Gabreels FJ. van Roosmalen T, et al. Am J Med Genet. 1999 Apr 2;83(4):264-7. doi: 10.1002/(sici)1096-8628(19990402)83:4<264::aid-ajmg6>3.0.co;2-r. Am J Med Genet. 1999. PMID: 10208159
X-linked mental retardation: evidence for a recent mutation in a five-generation family (MRX65) linked to the pericentromeric region.
Yntema HG, van den Helm B, Knoers NV, Smits AP, van Roosmalen T, Smeets DF, Mariman EC, van der Burgt I, van Bokhoven H, Ropers HH, Kremer H, Hamel BC. Yntema HG, et al. Among authors: van roosmalen t. Am J Med Genet. 1999 Jul 30;85(3):305-8. doi: 10.1002/(sici)1096-8628(19990730)85:3<305::aid-ajmg22>3.0.co;2-5. Am J Med Genet. 1999. PMID: 10398247
Longitudinal changes in cognitive-behavioral levels in three children with FRAXE.
Fisch GS, Carpenter NJ, Simensen R, Smits AP, van Roosmalen T, Hamel BC. Fisch GS, et al. Among authors: van roosmalen t. Am J Med Genet. 1999 May 28;84(3):291-2. doi: 10.1002/(sici)1096-8628(19990528)84:3<291::aid-ajmg25>3.0.co;2-2. Am J Med Genet. 1999. PMID: 10331610 No abstract available.