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Linde, H. van der

( H. van der Linde)


family mutation instability mouse deletion region chromosome expansion sequence transmission x syndrome allele fmr 1 gene length genet promoter triplet study genetic chorea genomic disease factor change premutation syndrome protein result model marker thyroid mouse promoter region trinucleotide 200 control chromosomes number disorder human analysis mechanism generation university oostra chromosome 14 q contraction chromosome 14 huntington family uk 1 instabilitie transcription basal function patient tract development basal ganglia mouse model fmrp expression individual dna replication agg interruptions primer position expression 11. thyroid transcription factor movement family nl 1 replication yeast families nl 1 element g 713t structure clone 1.2 mb fmr 1 r 243s onset neuron c 727a




2 Most Recent Publications

Mutations in TITF-1 are associated with benign hereditary chorea (Article)
Breedveld, G.J. Guala, A. Joosse, M. MacDonald, M.E. Krude, H. GrĂ¼ters, A. Dongen, J.W.F. van Danesino, C. Heutink, P. Oostra, B.A. Percy, A.K. Dure, L.S. Harper, P. Arts, W.F.M. Lazarou, L.P. Linde, H. van der Vries, B.B.A. de
2002-01-01
Instability of a (CGG)98 repeat in the Fmr1 promoter (Article)
Bontekoe, C.J.M. Bakker, C.E. Nieuwenhuizen, I.M. Linde, H. van der Lange, D. de Hirst, M.C. Oostra, B.A. Lans, W.J.
2001-01-01