Halley DJ - Search Results

1

Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype.

de Vries BB, Fryns JP, Butler MG, Canziani F, Wesby-van Swaay E, van Hemel JO, Oostra BA, Halley DJ, Niermeijer MF. de Vries BB, et al. Among authors: halley dj. J Med Genet. 1993 Sep;30(9):761-6. doi: 10.1136/jmg.30.9.761. J Med Genet. 1993. PMID: 8411072 Free PMC article.

2

Strategy for reliable prenatal detection of normal male carriers of the fragile X syndrome.

Halley D, Van Den Ouweland A, Deelen W, Verma I, Oostra B. Halley D, et al. Am J Med Genet. 1994 Jul 15;51(4):471-3. doi: 10.1002/ajmg.1320510435. Am J Med Genet. 1994. PMID: 7943022

3

The fragile-X syndrome: a growing gene causing familial intellectual disability.

De Vries LB, Halley DJ, Oostra BA, Niermeijer MF. De Vries LB, et al. Among authors: halley dj. J Intellect Disabil Res. 1994 Feb;38 ( Pt 1):1-8. doi: 10.1111/j.1365-2788.1994.tb00342.x. J Intellect Disabil Res. 1994. PMID: 8173220 Review.

4

Complex behavior of simple repeats: the fragile X syndrome.

Oostra BA, Halley DJ. Oostra BA, et al. Among authors: halley dj. Pediatr Res. 1995 Nov;38(5):629-37. doi: 10.1203/00006450-199511000-00001. Pediatr Res. 1995. PMID: 8552426 Review.

5

General overgrowth in the fragile X syndrome: variability in the phenotypic expression of the FMR1 gene mutation.

de Vries BB, Robinson H, Stolte-Dijkstra I, Tjon Pian Gi CV, Dijkstra PF, van Doorn J, Halley DJ, Oostra BA, Turner G, Niermeijer MF. de Vries BB, et al. Among authors: halley dj. J Med Genet. 1995 Oct;32(10):764-9. doi: 10.1136/jmg.32.10.764. J Med Genet. 1995. PMID: 8558551 Free PMC article.

6

Mental status of females with an FMR1 gene full mutation.

de Vries BB, Wiegers AM, Smits AP, Mohkamsing S, Duivenvoorden HJ, Fryns JP, Curfs LM, Halley DJ, Oostra BA, van den Ouweland AM, Niermeijer MF. de Vries BB, et al. Among authors: halley dj. Am J Hum Genet. 1996 May;58(5):1025-32. Am J Hum Genet. 1996. PMID: 8651263 Free PMC article.

7

Variable FMR1 gene methylation of large expansions leads to variable phenotype in three males from one fragile X family.

de Vries BB, Jansen CC, Duits AA, Verheij C, Willemsen R, van Hemel JO, van den Ouweland AM, Niermeijer MF, Oostra BA, Halley DJ. de Vries BB, et al. Among authors: halley dj. J Med Genet. 1996 Dec;33(12):1007-10. doi: 10.1136/jmg.33.12.1007. J Med Genet. 1996. PMID: 9004132 Free PMC article. Review.

8

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.

9

DNA testing for fragile X syndrome: implications for parents and family.

van Rijn MA, de Vries BB, Tibben A, van den Ouweland AM, Halley DJ, Niermeijer MF. van Rijn MA, et al. Among authors: halley dj. J Med Genet. 1997 Nov;34(11):907-11. doi: 10.1136/jmg.34.11.907. J Med Genet. 1997. PMID: 9391884 Free PMC article.

10

Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus.

Losekoot M, Hoogendoorn E, Olmer R, Jansen CC, Oosterwijk JC, van den Ouweland AM, Halley DJ, Warren ST, Willemsen R, Oostra BA, Bakker E. Losekoot M, et al. Among authors: halley dj. J Med Genet. 1997 Nov;34(11):924-6. doi: 10.1136/jmg.34.11.924. J Med Genet. 1997. PMID: 9391887 Free PMC article.

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