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Nellist, Mark, Brouwer, Rutger W W, Kockx, Christel E M, van Veghel-Plandsoen, Monique, Withagen-Hermans, Caroline, Prins-Bakker, Lida, Hoogeveen-Westerveld, Marianne, Mrsic, Alan, van den Berg, Mike M P, Koopmans, Anna E, de Wit, Marie-Claire, Jansen, Floor E, Maat-Kievit, Anneke J A, van den Ouweland, Ans, Halley, Dicky, de Klein, Annelies, van IJcken, Wilfred F J
Published in BMC medical genetics (25.02.2015)
Published in BMC medical genetics (25.02.2015)
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High Rate of Mosaicism in Tuberous Sclerosis Complex
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Published in American journal of human genetics (01.06.1999)
Published in American journal of human genetics (01.06.1999)
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Somatic mosaicism and clinical variation in tuberous sclerosis complex
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Published in The Lancet (British edition) (21.01.1995)
Published in The Lancet (British edition) (21.01.1995)
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Mutational spectrum of the TSC1 gene in a cohort of 225 tuberous sclerosis complex patients: no evidence for genotype-phenotype correlation
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Published in Journal of medical genetics (01.04.1999)
Published in Journal of medical genetics (01.04.1999)
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An unbalanced submicroscopic translocation t(8;16)(q24.3;p13.3)pat associated with tuberous sclerosis complex, adult polycystic kidney disease, and hypomelanosis of Ito
Eussen, Bert H J, Bartalini, Gabriella, Bakker, Lida, Balestri, Paolo, Di Lucca, Carmela, Van Hemel, Jan O, Dauwerse, Hans, van den Ouweland, Ans M W, Ris-Stalpers, Carrie, Verhoef, Senno, Halley, Dicky J J, Fois, Alberto
Published in Journal of medical genetics (01.04.2000)
Published in Journal of medical genetics (01.04.2000)
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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 gene
van den Ouweland, A M, de Vries, B B, Bakker, P L, Deelen, W H, de Graaff, E, van Hemel, J O, Oostra, B A, Niermeijer, M F, Halley, D J
Published in American journal of medical genetics (15.07.1994)
Published in American journal of medical genetics (15.07.1994)
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