Authors: Betz, RC Schoser, BGH Kasper, D Ricker, K Ramirez, A Stein, V Torbergsen, T Lee, YA Nothen, MM Wienker, TF Malin, JP Propping, P Reis, A Mortier, W Jentsch, TJ Vorgerd, M Kubisch, C

Citation: Rc. Betz et al., Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle inrippling muscle disease, NAT GENET, 28(3), 2001, pp. 218-219

Authors: Hildebrandt, F Rensing, C Betz, RC Sommer, U Birnbaum, S Imm, A Omran, H Leipoldt, M Otto, E

Citation: F. Hildebrandt et al., Establishing an algorithm for molecular genetic diagnostics in 127 families with juvenile nephronophthisis, KIDNEY INT, 59(2), 2001, pp. 434-445

Authors: Hillmer, AM Kruse, R Betz, RC Schumacher, J Heyn, U Propping, P Nothen, MM Cichon, S

Citation: Am. Hillmer et al., Variant 1859G -> A (Arg620Gln) of the "hairless" gene: Absence of association with papular atrichia or androgenetic alopecia, AM J HU GEN, 69(1), 2001, pp. 235-237

Authors: Bosse, K Betz, RC Lee, YA Wienker, TF Reis, A Kleen, H Propping, P Cichon, S Nothen, MM

Citation: K. Bosse et al., Localization of a gene for syndactyly type 1 to chromosome 2q34-q36, AM J HU GEN, 67(2), 2000, pp. 492-497

Authors: Betz, RC Lee, YA Bygum, A Brandrup, F Bernal, AI Toribio, J Alvarez, JI Kukuk, GM Ibsen, HHW Rasmussen, HB Wienker, TF Reis, A Propping, P Kruse, R Cichon, S Nothen, MM

Citation: Rc. Betz et al., A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3, AM J HU GEN, 66(6), 2000, pp. 1979-1983