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Year | Number of Results |
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1999 | 4 |
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Page 1
Palliative care for children: methodology for the development of a national clinical practice guideline.
BMC Palliat Care. 2023 Dec 1;22(1):193. doi: 10.1186/s12904-023-01293-3.
BMC Palliat Care. 2023.
PMID: 38041060
Free PMC article.
Review.
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
Item in Clipboard
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.
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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
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Localisation of a gene for non-specific X linked mental retardation (MRX46) to Xq25-q26.
Yntema HG, Hamel BC, Smits AP, van Roosmalen T, van den Helm B, Kremer H, Ropers HH, Smeets DF, van Bokhoven H.
Yntema HG, et al. Among authors: van roosmalen t.
J Med Genet. 1998 Oct;35(10):801-5. doi: 10.1136/jmg.35.10.801.
J Med Genet. 1998.
PMID: 9783701
Free PMC article.
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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
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Four families (MRX43, MRX44, MRX45, MRX52) with nonspecific X-linked mental retardation: clinical and psychometric data and results of linkage analysis.
Hamel BC, Smits AP, van den Helm B, Smeets DF, Knoers NV, van Roosmalen T, Thoonen GH, Assman-Hulsmans CF, Ropers HH, Mariman EC, Kremer H.
Hamel BC, et al. Among authors: van roosmalen t.
Am J Med Genet. 1999 Jul 30;85(3):290-304.
Am J Med Genet. 1999.
PMID: 10398246
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