Risk calculations for hereditary effects of ionizing radiation in humans F. Vogel Review Article Pages: 127 - 146
Genetic and blood coagulation characterization of “Swedish” families with von Willebrand's disease types I and III: New aspects of heredity Maria AnvretMargareta BlombäckAnn-Christine Thelander Original Investigations Pages: 147 - 154
Differential termination of primer extension: a novel, quantifiable method for detection of point mutations D. J. PickettsC. CameronDavid P. Lillicrap Original Investigations Pages: 155 - 157
Molecular characterization of genetic mutations in human lactate dehydrogenase (LDH) B (H) variant Kayoko SudoMasato MaekawaJun Toriumi Original Investigations Pages: 158 - 162
Detection of multiple cystic fibrosis mutations by reverse dot blot hybridization: a technology for carrier screening Fand F. ChehabJeff Wall Original Investigations Pages: 163 - 168
The polymorphism ApoB/4311 in patients with myocardial infarction and controls: the ECTIM study J. F. R. MoreelG. RoizesF. Cambien Original Investigations Pages: 169 - 175
Cytogenetic studies in motile sperm from normal men J. BenetA. GenescàC. Templado Original Investigations Pages: 176 - 180
Repair of human sperm chromosome aberrations in the hamster egg A. GenescàM. R. CaballínJ. Egozcue Original Investigations Pages: 181 - 186
Isolation and mapping of polymorphic cosmid clones used for sublocalization of the multiple endocrine neoplasia type 1 (MEN1) locus Catharina LarssonGünther WeberMagnus Nordenskjöld Original Investigations Pages: 187 - 193
Polymerase chain reaction amplification of two polymorphic simple repeat sequences within the von Willebrand factor gene: application to family studies in von Willebrand disease Anthony M. CummingJohn G. ArmstrongRichard T. Wensley Original Investigations Pages: 194 - 198
A new polymorphism of thyroxin-binding globulin in three African groups (Mali) with endemic nodular goitre J. ConstansM. T. RibouchonJ. Clayton Original Investigations Pages: 199 - 203
Estimation of the male and female mutation rates in Duchenne muscular dystrophy (DMD) B. MüllerC. DechantT. Grimm Original Investigations Pages: 204 - 206
Multipoint linkage analysis of the short arm of chromosome 11 in non-insulin dependent diabetes including maturity onset diabetes of youth S. O'RahillyP. PatelJ. S. Wainscoat Original Investigations Pages: 207 - 212
Variation in gene copy number and polymorphism of the human salivary amylase isoenzyme system in Caucasians Ruud A. BankEwald H. HettemaJan C. Pronk Original Investigations Pages: 213 - 222
Wiskott-Aldrich syndrome carrier detection with the hypervariable marker M27β G. de Saint BasileL. D. NotarangeloA. Fischer Original Investigations Pages: 223 - 228
The human fumarylacetoacetase gene: characterisation of restriction fragment length polymorphisms and identification of haplotypes in tyrosinemia type 1 and pseudodeficiency Helge RootweltEli Anne KvittingenRund Berger Original Investigations Pages: 229 - 233
Localization of the human insulin-like growth-factor-binding protein 4 gene to chromosomal region 17q12–21.1 Svetlana BajalicaSusanne V. AllanderCatharina Larsson Short Communications Pages: 234 - 236
Prenatal diagnosis of familial hypercholesterolemia caused by the “Lebanese” mutation at the low density lipoprotein receptor locus Ayeleth ReshefVardiella MeinerEran Leitersdorf Short Communications Pages: 237 - 239
Expression of RPS4X in fibroblasts from patients with structural aberrations of the X chromosome Walter JustClaudia GeerkensWalther Vogel Short Communications Pages: 240 - 242
Polymorphism in the RD (D6S45) gene Perrin C. WhiteJiri VitekPhyllis W. Speiser Short Communications Pages: 243 - 244
The occurrence of various non-ΔF508 CFTR gene mutations among Hungarian cystic fibrosis patients Margit NemetiJohn P. JohnsonElaine Louie Short Communications Pages: 245 - 246
Evidence for an ancestral alphoid domain on the long arm of human chromosome 2 Rosamaria AvarelloAntonio PediciniMarco Fraccaro Short Communications Pages: 247 - 249
Absence of p53 germ-line mutations in bilateral breast cancer patients Rosette LidereauThierry Soussi Short Communications Pages: 250 - 252
