The SOX10/Sox10 gene from human and mouse: sequence, expression, and transactivation by the encoded HMG domain transcription factor C. PuschElisabeth HustertG. Scherer Rapid Communication Pages: 115 - 123
Localization of a gene for incomplete X-linked congenital stationary night blindness to the interval between DXS6849 and DXS8023 in Xp11.23 N. T. Bech-HansenKym M. BoycottWilliam G. Pearce Original investigation Pages: 124 - 130
Characterization of the human synaptogyrin gene family Darek KedraHua-Qin PanJ. P. Dumanski Original Investigation Pages: 131 - 141
Japanese juvenile retinoschisis is caused by mutations of the XLRS1 gene Y. HottaKeiko FujikiNoriyuki Azuma Original Investigation Pages: 142 - 144
Phenotypic variation in a family with mutations in two Hirschsprung-related genes (RET and endothelin receptor B) P.-J. SvenssonMaria AnvretAgneta Nordenskjöld Original Investigation Pages: 145 - 148
Missense mutation and hexanucleotide duplication in the PAX2 gene in two unrelated families with renal-coloboma syndrome (MIM 120330) K. DevriendtGert MatthijsAnita Leys Original Investigation Pages: 149 - 153
A high proportion of mutations in the BRCA1 gene in German breast/ovarian cancer families with clustering of mutations in the 3′ third of the gene Juan DongJenny Chang-ClaudeBrigitte Royer-Pokora Original Investigation Pages: 154 - 161
Mutations in the pterin-4α-carbinolamine dehydratase (PCBD) gene cause a benign form of hyperphenylalaninemia B. ThönyF. NeuheiserN. Blau Original Investigation Pages: 162 - 167
Nine novel germline mutations of STK11 in ten families with Peutz-Jeghers syndrome Hidewaki NakagawaKumiko KoyamaY. Nakamura Original Investigation Pages: 168 - 172
Molecular characterization and delineation of subtle deletions in de novo “balanced” chromosomal rearrangements Arun KumarLaurie A. BeckerS. Schwartz Original Investigation Pages: 173 - 178
A novel splice site mutation in the tissue inhibitor of the metalloproteinases-3 gene in Sorsby’s fundus dystrophy with unusual clinical features Yoshiaki TabataYasushi IsashikiN. Ohba Original Investigation Pages: 179 - 182
Genetics strongly determines the wall thickness of the left and right carotid arteries F. ZannadS. VisvikisG. Siest Original Investigation Pages: 183 - 188
Molecular cloning of the chromosomal breakpoint in the LIS1 gene of a patient with isolated lissencephaly and balanced t(8;17) H. KurahashiMichiko SakamotoYusuke Nakamura Original Investigation Pages: 189 - 192
The Usher syndrome in the Lebanese population and further refinement of the USH2A candidate region Myrna SaoudaAhmad MansourR. Slim Original Investigation Pages: 193 - 198
Linkage disequilibrium and linkage analysis of the glucose-6-phosphatase gene L.-J. C. WongMin-Hui LiangChing-Wan Lam Original Investigation Pages: 199 - 203
Extensive polymorphism of the FUT2 gene in an African (Xhosa) population of South Africa Yuhua LiuYoshiro KodaH. Kimura Original Investigation Pages: 204 - 210
A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus Kenneth K. KiddBharti MorarJudith R. Kidd Original Investigation Pages: 211 - 227
Variation of site-specific methylation patterns in the factor VIII (F8C) gene in human sperm DNA David S. MillarMichael KrawczakD. N. Cooper Original Investigation Pages: 228 - 233
An ecological study of association between coronary heart disease mortality rates in men and the relative frequencies of common allelic variations in the gene coding for apolipoprotein E J. H. StengårdKenneth M. WeissCharles F. Sing Original investigation Pages: 234 - 241
Genotype/phenotype correlation in affected individuals of a family with a deletion of the entire coding sequence of the connexin 32 gene P. J. AinsworthC. F. BoltonA. F. Hahn Original investigation Pages: 242 - 244
Molecular characterization and mutational analysis of the human B17 subunit of the mitochondrial respiratory chain complex I J. SmeitinkJ. LoeffenL. van den Heuvel Original Investigation Pages: 245 - 250
Gene therapy for neurological disorders and brain tumors: E. A. Chiocca and X. O. Breakefield (Editors) P. R. Lowenstein Book Review Pages: 251 - 252