The genetics of primary torsion dystonia Ulrich MüllerKenneth G. Kupke Review Article Pages: 107 - 115
Neurofibromatosis-1: a maximum likelihood estimation of mutation rate Maurizio ClementiGuido BarbujaniRomano Tenconi Original Investigations Pages: 116 - 118
Cloning and sequence analysis of the human parathyroid hormone gene region A. ReisW. HechtJ. Schmidtke Original Investigations Pages: 119 - 124
Molecular cloning of human preproacrosin cDNA Ibrahim M. AdhamUwe KlemmWolfgang Engel Original Investigations Pages: 125 - 128
Detection of β-thalassemia mutations in the Chinese using amplified DNA from dried blood specimens Shu-zhen HuangXia-di ZhouYi-tao Zeng Original Investigations Pages: 129 - 131
An association between α1-antitrypsin phenotype and chronic liver disease Yosuke KishimotoSadako YamadaChisato Hirayama Original Investigations Pages: 132 - 136
A monoclonal antibody against human vitamin-D-binding protein for the analysis of genetic variation in the group-specific component system (Gc) Rainer HoffmannAndreas BraunHartwig Cleve Original Investigations Pages: 137 - 146
Regional assignment of 41 human DNA fragments on chromosome 7 by means of a somatic cell hybrid panel Anke JobsDirk Klein-BöltingKarl-Heinz Grzeschik Original Investigations Pages: 147 - 150
A “new” genetic polymorphism of a human serum protein: inter-alpha-trypsin-inhibitor Ulrike VogtHartwig Cleve Original Investigations Pages: 151 - 154
Parental age and seasonal variation in the births of children with sporadic retinoblastoma: a mutation-epidemiologic study E. MatsunagaK. MinodaM. S. Sasaki Original Investigations Pages: 155 - 158
Meiotic and sperm chromosome studies in a reciprocal translocation t(1;2)(q32;q36) C. TempladoJ. NavarroJ. Egozcue Original Investigations Pages: 159 - 162
A probable sex difference in mutation rates in ornithine transcarbamylase deficiency Catherine Bonaïti-PelliéAnna PeletArnold Munnich Original Investigations Pages: 163 - 166
Carrier detection in a partially dominant X-linked disease: ornithine transcarbamylase deficiency Anna PeletAgnès RotigArnold Munnich Original Investigations Pages: 167 - 171
Search for chromosomal variations among gas-exposed persons in Bhopal H. K. GoswamiManoj ChandorkarP. N. Sharma Original Investigations Pages: 172 - 176
Dual genotype in cutaneous T-cell lymphomas and pseudolymphomas Y. J. BignonP. SouteyrandR. Plagne Original Investigations Pages: 177 - 178
Extent and high frequency of a short conversion between the human Aγ and Gγ fetal globin genes J. StarckR. BouhassJ. Godet Original Investigations Pages: 179 - 184
Monocyte-derived neutrophil chemotactic factor (MDNCF/IL-8) resides in a gene cluster along with several other members of the platelet factor 4 gene superfamily William S. ModiMichael DeanStephen J. O'Brien Original Investigations Pages: 185 - 187
The distribution of the Hb Constant Spring gene in Southeast Asian populations Marion LaigMichael PapeNaret Mularlee Original Investigations Pages: 188 - 190
Chromosomal damage in peripheral blood lymphocytes of patients treated for testicular cancer Eva van den Berg-de RuiterBauke de JongDirk T. Sleijfer Original Investigations Pages: 191 - 194
Molecular basis of β-thalassemia in Turkey: detection of rare mutations by direct sequencing C. Aulehla-ScholzS. BasaranJ. Horst Original Investigations Pages: 195 - 197
Genotype-phenotype correlations in XX males and their bearing on current theories of sex determination M. A. Ferguson-SmithA. CookeJ. L. Tolmie Short Communications Pages: 198 - 202
Non-existence of a tight association between a 444leucine to proline mutation and phenotypes of Gaucher disease: high frequency of a NciI polymorphism in the non-neuronopathic form Mitsuo MasunoShunji TomatsuTadao Orii Short Communications Pages: 203 - 206
A normal male with an inherited deletion of one exon within the DMD gene Magnus NordenskjöldLouise NicholsonLisa Stolpe Short Communications Pages: 207 - 209
In situ mapping of the muscle-specific form of phosphoglycerate mutase gene to human chromosome 7p12-7p13 J. Castella-EscolaM. G. MatteiM. Cohen-Solal Short Communications Pages: 210 - 212
A new electrophoretically distinguishable variant of human diaphorase locus 3(DIA3): DIA3 6-1 Ryszard Pawlowski OriginalPaper Pages: 213 - 213
MspI polymorphic site in intron 22 of the factor VIII gene in the Japanese population Hiroshi InabaMichio FujimakiStylianos E. Antonarakis OriginalPaper Pages: 214 - 215
No significant relationship between age and frequency of chromosome lesions in mentally retarded individuals with or without the fragile X syndrome Merlin G. Butler Letter to the Editors Pages: 216 - 217
