Analysis of a paracentric inversion in human oocytes: nonhomologous pairing in pachytene E.Y. ChengY.J. ChenS.M. Gartler Original Investigation Pages: 191 - 196
Genetic contribution of the BAT2 gene microsatellite polymorphism to the age-at-onset of insulin-dependent diabetes mellitus M. HashimotoN. NakamuraM. Nishimura Original Investigation Pages: 197 - 199
Novel and recurrent mutations in the tyrosinase gene and the P gene in the German albino population L. PassmoreB. Kaesmann-Kellner B. Weber Original Investigation Pages: 200 - 210
Alpha-tectorin involvement in hearing disabilities: one gene – two phenotypes J. BalciunieneN. DahlE.E. Jazin Original Investigation Pages: 211 - 216
Isolation of CAG/CTG repeats from within the chromosome 2p21-p24 locus for autosomal dominant spastic paraplegia (SPG4) by YAC fragmentation J. Del-FaveroD. GoossensC. Van Broeckhoven Original Investigation Pages: 217 - 225
Dopa-responsive dystonia induced by a recessive GTP cyclohydrolase I mutation W.-L. HwuP.-J. WangY.-M. Lee Original Investigation Pages: 226 - 230
DGGE screening of PKD1 gene reveals novel mutations in a large cohort of 146 unrelated patients R.A. PerrichotB. MercierC. Ferec Original Investigation Pages: 231 - 239
A mutation in GLUT2, not in phosphorylase kinase subunits, in hepato-renal glycogenosis with Fanconi syndrome and low phosphorylase kinase activity B. BurwinkelS.A. SanjadM.W. Kilimann Original Investigation Pages: 240 - 243
Molecular genetics of human prion diseases in Germany O. WindlA. GieseH.A. Kretzschmar Original Investigation Pages: 244 - 252
Linkage of interleukin 6 locus to human osteopenia by sibling pair analysis N. OtaS.C. HuntM. Emi Original Investigation Pages: 253 - 257
Rapid FMR1-protein analysis of fetal blood: an enhancement of prenatal diagnostics N. LambirisH. PetersR. Willemsen Original Investigation Pages: 258 - 260
Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM K.L. FriendD. CrimminsR.I. Richards Original Investigation Pages: 261 - 265
Relationship between clinical phenotype, semen parameters and aneuploidy frequency in sperm nuclei of 50 infertile males Nathalie RivesAlexia Saint ClairBertrand Macé Original Investigation Pages: 266 - 272
Duplication of 7p12.1-p13, including GRB10 and IGFBP1, in a mother and daughter with features of Silver-Russell syndrome C.A. JoyceA. SharpI.K. Temple Original Investigation Pages: 273 - 280
Vitamin D receptor polymorphisms as markers in prostate cancer L. Correa-CerroP. BerthonW. Vogel Original Investigation Pages: 281 - 287
Reorganization of the sex-determining pathway with the evolution of placentation U. Wolf Food For Thought Pages: 288 - 292