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A prospective 10 year follow up study of patients with neurofibromatosis type 1.
Cnossen MH, de Goede-Bolder A, van den Broek KM, Waasdorp CM, Oranje AP, Stroink H, Simonsz HJ, van den Ouweland AM, Halley DJ, Niermeijer MF. Cnossen MH, et al. Among authors: halley dj. Arch Dis Child. 1998 May;78(5):408-12. doi: 10.1136/adc.78.5.408. Arch Dis Child. 1998. PMID: 9659085 Free PMC article.
Deletions spanning the neurofibromatosis type 1 gene: implications for genotype-phenotype correlations in neurofibromatosis type 1?
Cnossen MH, van der Est MN, Breuning MH, van Asperen CJ, Breslau-Siderius EJ, van der Ploeg AT, de Goede-Bolder A, van den Ouweland AM, Halley DJ, Niermeijer MF. Cnossen MH, et al. Among authors: halley dj. Hum Mutat. 1997;9(5):458-64. doi: 10.1002/(SICI)1098-1004(1997)9:5<458::AID-HUMU13>3.0.CO;2-1. Hum Mutat. 1997. PMID: 9143927
The fragile X syndrome.
de Vries BB, Halley DJ, Oostra BA, Niermeijer MF. de Vries BB, et al. Among authors: halley dj. J Med Genet. 1998 Jul;35(7):579-89. doi: 10.1136/jmg.35.7.579. J Med Genet. 1998. PMID: 9678703 Free PMC article. Review.
Screening and diagnosis for the fragile X syndrome among the mentally retarded: an epidemiological and psychological survey. Collaborative Fragile X Study Group.
de Vries BB, van den Ouweland AM, Mohkamsing S, Duivenvoorden HJ, Mol E, Gelsema K, van Rijn M, Halley DJ, Sandkuijl LA, Oostra BA, Tibben A, Niermeijer MF. de Vries BB, et al. Among authors: halley dj. Am J Hum Genet. 1997 Sep;61(3):660-7. doi: 10.1086/515496. Am J Hum Genet. 1997. PMID: 9326332 Free PMC article.
Screening with the FMR1 protein test among mentally retarded males.
de Vries BB, Mohkamsing S, van den Ouweland AM, Halley DJ, Niermeijer MF, Oostra BA, Willemsen R. de Vries BB, et al. Among authors: halley dj. Hum Genet. 1998 Oct;103(4):520-2. doi: 10.1007/s004390050860. Hum Genet. 1998. PMID: 9856500
199 results