Clinical features of facioscapulohumeral muscular dystrophy 2 von DE GREEF, J. C, LEMMERS, R. J. L. F, DESNUELLE, C, SPULER, S, TARNOPOLSKY, M, VENANCE, S. L, FRANTS, R. R, VAN DER MAAREL, S. M, TAWIL, R, CAMANO, P, DAY, J. W, SACCONI, S, DUNAND, M, VAN ENGELEN, B. G. M, KIURU-ENARI, S, PADBERG, G. W, ROSA, A. L

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Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigations von Voermans, N. C., van der Bilt, R. C., IJspeert, J., Hogrel, J. Y., Jeanpierre, M., Behin, A., Laforet, P., Stojkovic, T., van Engelen, B. G., Padberg, G. W., Sacconi, S., Lemmers, R. J. L. F., van der Maarel, S. M., Eymard, B., Bassez, G.

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Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4 von DEAK, K. L, LEMMERS, R. J. L. F, STAJICH, J. M, KLOOSTER, R, TAWIL, R, FRANTS, R. R, SPEER, M. C, VAN DER MAAREL, S. M, GILBERT, J. R

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Possible phenotypic dosage effect in patients compound heterozygous for FSHD-sized 4q35 alleles von WOHLGEMUTH, M, LEMMERS, R. J, VAN DER KOOI, E. L, VAN DER WIELEN, M. J, VAN OVERVELD, P. G, DAUWERSE, H, BAKKER, E, FRANTS, R. R, PADBERG, G. W, VAN DER MAAREL, S. M

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FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patients von Rijkers, T, Deidda, G, van Koningsbruggen, S, van Geel, M, Lemmers, R J L F, van Deutekom, J C T, Figlewicz, D, Hewitt, J E, Padberg, G W, Frants, R R, van der Maarel, S M

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Homozygosity for autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) does not result in a more severe phenotype von Tonini, M M O, Pavanello, R C M, Gurgel-Giannetti, J, Lemmers, R J, van der Maarel, S M, Frants, R R, Zatz, M

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D4F104S1 deletion in facioscapulohumeral muscular dystrophy: Phenotype, size, and detection von LEMMERS, R. J. L. F, OSBORN, M, HAAF, T, ROGERS, M, FRANTS, R. R, PADBERG, G. W, COOPER, D. N, VAN DER MAAREL, S. M, UPADHYAYA, M

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De Novo Facioscapulohumeral Muscular Dystrophy: Frequent Somatic Mosaicism, Sex-Dependent Phenotype, and the Role of Mitotic Transchromosomal Repeat Interaction between Chromosomes... von van der Maarel, Silvère M., Deidda, Giancarlo, Lemmers, Richard J.L.F., van Overveld, Petra G.M., van der Wielen, Michiel, Hewitt, Jane E., Sandkuijl, Lodewijk, Bakker, Bert, van Ommen, Gert-Jan B., Padberg, George W., Frants, Rune R.

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Evidence for Subtelomeric Exchange of 3.3 kb Tandemly Repeated Units between Chromosomes 4q35 and 10q26: Implications for Genetic Counselling and Etiology of FSHD1 von van Deutekom, Judith C. T., Bakker, Egbert, Lemmers, Richard J. L. F., van der Wielen, Michiel J. R., Bik, Elsa, Hofker, Marten H., Padberg, George W., Frants, Rune R.

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A focal domain of extreme demethylation within D4Z4 in FSHD2 von HARTWECK, Lynn M, ANDERSON, Lindsey J, LEMMERS, Richard J, DANDAPAT, Abhijit, TOSO, Erik A, DALTON, Joline C, TAWIL, Rabi, DAY, John W, VAN DER MAAREL, Silvère M, KYBA, Michael

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Inter-and Intrachromosomal Sub-Telomeric Rearrangements on 4q35: Implications for Facioscapulohumeral Muscular Dystrophy (FSHD) Aetiology and Diagnosis von Lemmers, Richard J. L. F., van der Maarel, Silvère M., van Deutekom, Judith C. T., van der Wielen, Michiel J. R., Deidda, Giancarlo, Dauwerse, Hans G., Hewitt, Jane, Hofker, Marten, Bakker, Egbert, Padberg, George W., Frants, Rune R.

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Rapid and accurate diagnosis of facioscapulohumeral muscular dystrophy von Lemmers, R.J.L.F., van der Wielen, M.J.R., Bakker, E., Frants, R.R., van der Maarel, S.M.

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Identification of the First Gene (FRG1) from the FSHD Region on Human Chromosome 4q35 von van Deutekom, Judith C. T., Lemmers, Richard J. L. F., Grewal, Prabhjit K., van Geel, Michel, Romberg, Silke, Dauwerse, Hans G., Wright, Tracy J., Padberg, George W., Hofker, Marten H., Hewitt, Jane E., Frants, Rune R.

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Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter von Könst, Andrea A.M, Lemmers, Richard J.L.F, Oudejans, Cees B.M, Fonds, Dafna, Leegwater, Peter A.J, Vermeulen, Gerre, Pronk, Jan C, van Berkel, Carola G.M, Visser, Allerdien, Mobach, Dragosh, van der Knaap, Marjo S, Schutgens, Ruud B.H, Naidu, Sakkubai, Mulders, Joyce, Kersbergen, Paula, Frants, Rune R

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A new dosage test for subtelomeric 4;10 translocations improves conventional diagnosis of facioscapulohumeral muscular dystrophy (FSHD) von van der Maarel, Silvère M, Deidda, Giancarlo, Lemmers, Richard J L F, Bakker, Egbert, van der Wielen, Michiel J R, Sandkuijl, Lodewijk, Hewitt, Jane E, Padberg, George W, Frants, Rune R

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Contractions of D4Z4 on 4qB Subtelomeres Do Not Cause Facioscapulohumeral Muscular Dystrophy von Lemmers, Richard J. F.L., Wohlgemuth, Mariëlle, Frants, Rune R., Padberg, George W., Morava, Eva, van der Maarel, Silvère M.

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Interchromosomal repeat array interactions between chromosomes 4 and 10: a model for subtelomeric plasticity von VAN OVERVELD, Petra G. M, LEMMERS, Richard J. F. L, DEIDDA, Giancarlo, SANDKUIJL, Lodewijk, PADBERG, George W, FRANTS, Rune R, VAN DER MAAREL, Silvère M

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Het voorkomen van de Kamsalamander in Weerterbos, Ringselven en Kruispeel von P. Lemmers & R. Krekels, J. Veldman

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GENERATOR WITH MOISTURE SEALS von LEMMERS, JR., Glenn C

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GENERATOR WITH MOISTURE SEALS von Lemmers, JR., Glenn C

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