Microlesions and polymorphisms in the Duchenne/Becker muscular dystrophy gene Frauke RininslandJochen Reiss Review Article Pages: 111 - 116
Angiotensin I-converting enzyme (ACE): estimation of DNA haplotypes in unrelated individuals using denaturing gradient gel blots Alessandro DoriaJ. H. WarramA. S. Krolewski Original Investigation Pages: 117 - 123
Geographical distribution of haplotypes in Swedish families with Huntington's disease Elisabeth AlmqvistSusan AndrewMaria Anvret Original Investigation Pages: 124 - 128
Molecular basis for subtypic differences of the “a” subunit of coagulation factor XIII with description of the genesis of the subtypes Koichi SuzukiMisa IwataYasuhiko Mizoi Original Investigation Pages: 129 - 135
Mutation analysis of a Sandhoff disease patient in the Maronite community in Cyprus Yoji HaraPanos IoannouKunihiko Suzuki Original Investigation Pages: 136 - 140
Linkage analysis of X-linked cleft palate and ankyloglossia in Manitoba Mennonite and British Columbia Native kindreds Sharon M. GorskiKaren J. AdamsPaul J. Goodfellow Original Investigation Pages: 141 - 148
Molecular cytogenetic analysis of a duplication Xp in a male: further delineation of a possible sex influencing region on the X chromosome P. Nagesh RaoKurt KlinepeterMark J. Pettenati Original Investigation Pages: 149 - 153
Identification of three novel mutations in the CFTR gene using temperature-optimized non-radioactive conditions for SSCP analysis Klaus GradeIngrid GrunewaldCharles Coutelle Original Investigation Pages: 154 - 158
Exclusion of ferritins and iron-responsive element (IRE)-binding proteins as candidates for the hemochromatosis gene H. ZhengD. BhavsarJ. Drysdale Original Investigation Pages: 159 - 164
Linkage disequilibrium relationships among four polymorphisms within the human fibrinogen gene cluster Russell E. BaumannAgnes H. Henschen Original Investigation Pages: 165 - 170
Balanced autosomal translocations and ovarian dysgenesis Rossella TuplerLaura BarbieratoPaola Maraschio Original Investigation Pages: 171 - 176
Exonic polymorphisms in the protein C gene: interethnic comparison between Caucasians and Asians Woei TsayJudith S. GreengardJohn H. Griffin Original Investigation Pages: 177 - 178
Familial resemblance for immunoglobulin levels I. B. BoreckiM. McGueD. C. Rao Original Investigation Pages: 179 - 185
Chromosomal localization of the human histamine H1-receptor gene Maryvonne Le ConiatElisabeth TraiffortRoland Berger Short Communication Pages: 186 - 188
Polymorphisms of the apolipoprotein and angiotensin converting enzyme genes in young North Karelian patients with coronary heart disease Helena E. MiettinenKai KorpelaKimmo Kontula Short Communication Pages: 189 - 192
Genetic fine localization of the arrestin (S-antigen) gene 4 cM distal from D2S172 Diana ValverdeMònica BayésMontserrat Baiget Short Communication Pages: 193 - 194
Parathyroid Water Clear Cell Hyperplasia, an O-allele associated condition Gunilla HedbäckAnders Odén Short Communication Pages: 195 - 197
A characteristic sequence of trisomies starting with trisomy 7 in benign thyroid tumors Gazanfer BelgeBrita ThodeJörn Bullerdiek Short Communication Pages: 198 - 202
Variability in allelic DNA methylation in spermatozoa Stefan KochanekDoris RenzWalter Doerfler Short Communication Pages: 203 - 206
Deletion polymorphism in the gene for angiotensin converting enzyme is associated with elevated fasting blood glucose levels Adriana ZingoneAndrea DominijanniNicola Perrotti Short Communication Pages: 207 - 209
Sublocalization of a locus at 3p21.3–23 predisposing to hereditary nonpolyposis colon cancer Pia TannergårdEugene ZabarovskyAnnika Lindblom Short Communication Pages: 210 - 214
An MspI polymorphism in the X-specific region proximal to the pseudoautosomal boundary. A new example of a unique “African” marker? F. CrucianiD. SellittoR. Scozzari DNA Variants Pages: 215 - 216
