The fragile X gene and its functionOOSTRA, B. A; CHIURAZZI, P.Clinical genetics. 2001, Vol 60, Num 6, pp 399-408, issn 0009-9163Article

The X chromosome and fragile X mental retardationOOSTRA, B. A; WILLEMSEN, R.Cytogenetic and genome research. 2003, Vol 99, Num 1-4, pp 257-264, issn 1424-8581, 8 p.Article

Animal model for fragile X syndrome : Gene therapy of single-gene disordersOOSTRA, B. A; HOOGEVEEN, A. T.Annals of medicine (Helsinki). 1997, Vol 29, Num 6, pp 563-567, issn 0785-3890Conference Paper

Complex behavior of simple repeats : the fragile X syndromeOOSTRA, B. A; HALLEY, D. J. J.Pediatric research. 1995, Vol 38, Num 5, pp 629-637, issn 0031-3998Article

CGG repeat in the FMR1 gene: size mattersWILLEMSEN, R; LEVENGA, J; OOSTRA, B. A et al.Clinical genetics. 2011, Vol 80, Num 3, pp 214-225, issn 0009-9163, 12 p.Article

The FMR1 Gene and Fragile X-Associated Tremor/Ataxia SyndromeBROUWER, J. R; WILLEMSEN, R; OOSTRA, B. A et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2009, Vol 150, Num 6, pp 782-798, issn 1552-4841, 17 p.Article

The fragile X syndrome: isolation of the FMR-1 gene and characterization of the fragile X mutationOOSTRA, B. A; VERKERK, A. J. M. H.Chromosoma (Berlin. Print). 1992, Vol 101, Num 7, pp 381-387, issn 0009-5915Article

RFLP for the human retinoic acid receptor gene RAR-βDATSON, N. A; VAN DER SAAG, P. T; OOSTRA, B. A et al.Nucleic acids research. 1989, Vol 17, Num 21, issn 0305-1048, 8897 [1 p.]Article

Studying the genetics of Hirschsprung's disease: unraveling an oligogenic disorderBROOKS, A. S; OOSTRA, B. A; HOFSTRA, R. M. W et al.Clinical genetics. 2005, Vol 67, Num 1, pp 6-14, issn 0009-9163, 9 p.Article

Genetic risk factors for cerebral small-vessel disease in hypertensive patients from a genetically isolated populationSCHUUR, M; VAN SWIETEN, J. C; VROOMAN, H et al.Journal of neurology, neurosurgery and psychiatry. 2011, Vol 82, Num 1, pp 41-44, issn 0022-3050, 4 p.Article

Menopause impacts the relation of plasma adiponectin levels with the metabolic syndromeHENNEMAN, P; JANSSENS, A. C. J. W; ZILLIKENS, M. C et al.Journal of internal medicine. 2010, Vol 267, Num 4, pp 402-409, issn 0954-6820, 8 p.Article

Altered hypothalamus-pituitary-adrenal gland axis regulation in the expanded CGG-repeat mouse model for fragile X-associated tremor/ataxia syndromeBROUWER, J. R; SEVERIJNEN, E; DE JONG, F. H et al.Psychoneuroendocrinology. 2008, Vol 33, Num 6, pp 863-873, issn 0306-4530, 11 p.Article

Heritability of fasting glucose levels in a young genetically isolated populationSANTOS, R. L. P; ZILLIKENS, M. C; RIVADENEIRA, F. R et al.Diabetologia (Berlin). 2006, Vol 49, Num 4, pp 667-672, issn 0012-186X, 6 p.Article

Instability of a (CGG)₉₈ repeat in the Fmr1 promoterBONTEKOE, C. J. M; BAKKER, C. E; NIEUWENHUIZEN, I. M et al.Human molecular genetics (Print). 2001, Vol 10, Num 16, pp 1693-1699, issn 0964-6906Article

The fragile X-related proteins FXR1P and FXR2P contain a functional nucleolar-targeting signal equivalent to the HIV-1 regulatory proteinsTAMANINI, F; KIRKPATRICK, L. L; SCHONKEREN, J et al.Human molecular genetics (Print). 2000, Vol 9, Num 10, pp 1487-1493, issn 0964-6906Article

Clinical and genetic studies on 12 preaxial polydactyly families and refinement of the localisation of the gene responsible to a 1.9 cM region on chromosome 7q36ZGURICAS, J; HEUS, H; HEREDERO-BAUTE, L et al.Journal of medical genetics. 1999, Vol 36, Num 1, pp 32-40, issn 0022-2593Article

Screening for the fragile X syndrome among the mentally retarded: a clinical studyDE VRIES, B. B. A; MOHKAMSING, S; NIERMEIJER, M. F et al.Journal of medical genetics. 1999, Vol 36, Num 6, pp 467-470, issn 0022-2593Article

FMRP expression as a potential prognostic indicator in fragile X syndromeTASSONE, F; HAGERMAN, R. J; IKLE, D. N et al.American journal of medical genetics. 1999, Vol 84, Num 3, pp 250-261, issn 0148-7299Article

The fragile X syndromeDE VRIES, B. B. A; HALLEY, D. J. J; OOSTRA, B. A et al.Journal of medical genetics. 1998, Vol 35, Num 7, pp 579-589, issn 0022-2593Article

Screening with the FMR1 protein test among mentally retarded malesDE VRIES, B. B. A; MOHKAMSING, S; VAN DEN OUWELAND, A. M. W et al.Human genetics. 1998, Vol 103, Num 4, pp 520-522, issn 0340-6717Article

A gene for nonspecific X-linked mental retardation (MRX41) is located in the distal segment of Xq28HAMEL, B. C. J; KREMER, H; WESBY-VAN SWAAY, E et al.American journal of medical genetics. 1996, Vol 64, Num 1, pp 131-133, issn 0148-7299Article

Fragile X founder chromosomes in Italy : A few initial events and possible explanation for their heterogeneityCHIURAZZI, P; GENUARDI, M; OOSTRA, B. A et al.American journal of medical genetics. 1996, Vol 64, Num 1, pp 209-215, issn 0148-7299Article

A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndromeMEIJER, H; DE GRAAFF, E; MERCKX, D. M. L et al.Human molecular genetics (Print). 1994, Vol 3, Num 4, pp 615-620, issn 0964-6906Article

DNA diagnosis of the fragile X syndrome in a series of 236 mentally retarded subjects and evidence for a reversal of mutation in the FMR-1 geneVAN DEN OUWELAND, M. W; DE VRIES, B. B. A; BAKKER, P. L. G et al.American journal of medical genetics. 1994, Vol 51, Num 4, pp 482-485, issn 0148-7299Article

Dinucleotide repeat polymorphism at D11S994 locusBONTEKOE, C. J. M; DE GRAAFF, E; BREEDVELD, G. J et al.Human molecular genetics (Print). 1993, Vol 2, Num 10, issn 0964-6906, p. 1747Article