Carrier detection and prenatal diagnosis of alpha-thalassemia of Southeast Asian deletion by polymerase chain reaction Tsang-Ming KoLi-Hui TsengTzu-Yao Lee Original Investigations Pages: 245 - 248
Parental origin and germline mosaicism of deletions and duplications of the dystrophin gene: a European study Anthonie J. van EssenStephen AbbsLeo P. ten Kate Original Investigations Pages: 249 - 257
Birth and population prevalence of Duchenne muscular dystrophy in the Netherlands Anthonie J. van EssenH. F. M. BuschLeo P. ten Kate Original Investigations Pages: 258 - 266
Heterozygote deficiency, population substructure and their implications in DNA fingerprinting Ranajit ChakrabortyLi Jin Original Investigations Pages: 267 - 272
Ewing's tumor X mouse hybrids expressing the MIC2 antigen: analyses using fluorescence CDD-banding and non-isotopic ISH M. DworzakC. StockP. F. Ambros Original Investigations Pages: 273 - 278
Preferential mutation of the neurofibromatosis type 1 gene in paternally derived chromosomes Karen StephensLucille KayesRoberta A. Pagon Original Investigations Pages: 279 - 282
Single-strand conformation polymorphism (SSCP) analysis of exon 11 of the CFTR gene reliably detects more than one third of non-ΔF508 mutations in German cystic fibrosis patients Juliane PliethFrauke RininslandJochen Reiss Original Investigations Pages: 283 - 287
Mosaicism in 45,X Turner syndrome: does survival in early pregnancy depend on the presence of two sex chromosomes? K. R. HeldS. KerberH. W. Goedde Original Investigations Pages: 288 - 294
Chromosomal localization of the human glycoasparaginase gene to 4q32–q33 Christine MorrisNora HeisterkampIlkka Mononen Original Investigations Pages: 295 - 297
Exclusion map of Salla disease: attempts to localize the disease gene using a computer program Leena HaatajaJohanna SchlentkerPertti Aula Original Investigations Pages: 298 - 300
Sib pair linkage analysis of renin gene haplotypes in human essential hypertension Xavier JeunemaitreBrigitte RigatPierre Corvol Original Investigations Pages: 301 - 306
Apolipoprotein E phenotypes and hyperlipidemia in patients under maintenance hemodialysis Giso FeussnerStephan WeyReinhard Ziegler Original Investigations Pages: 307 - 312
Cloning of the human α2-macroglobulin gene and detection of mutations in two functional domains: the bait region and the thiolester site W. PollerJ.-P. FaberK. Olek Original Investigations Pages: 313 - 319
Heterogeneity of mutations in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria Samia BoulechfarVasco Da SilvaHubert de Verneuil Original Investigations Pages: 320 - 324
A 27-bp deletion from one allele of the type III collagen gene (COL3A1) in a large family with Ehlers-Danlos syndrome type IV A. J. RichardsJ. C. LloydF. M. Pope Original Investigations Pages: 325 - 330
A family with RP3 type of X-linked retinitis pigmentosa: an association with ciliary abnormalities Dieuwke B. van DorpAlan F. WrightElizabeth M. Bleeker-Wagemakers Original Investigations Pages: 331 - 334
Estimating the stability of the proposed imprinted state of the fragile-X mutation when transmitted by females Peter J. FolletteCharles D. Laird Original Investigations Pages: 335 - 343
Distribution of ADH2 and ALDH2 genotypes in different populations H. W. GoeddeD. P. AgarwalA. Czeizel Short Communications Pages: 344 - 346
Molecular abnormality of a Japanese glucose-6-phosphate dehydrogenase variant (G6PD Tokyo) associated with hereditary non-spherocytic hemolytic anemia Akira HironoHisaichi FujiiShiro Miwa Short Communications Pages: 347 - 348
Localisation of the gene for Norrie disease to between DXS7 and DXS426 on Xp S. LindsayD. L. ThiseltonS. S. Bhattacharya Short Communications Pages: 349 - 350
Familial synovial chondromatosis combined with dwarfism Jochen FelbelUrsula GresserNepomuk Zöllner Clinical Case Report Pages: 351 - 354
A rare genetic variant of the T cell receptor gamma joining segment TRGJI M. WeillX. M. ZhangM.-P. Lefranc OriginalPaper Pages: 355 - 355
Dinucleotide (CA/GT) repeat polymorphism in intron 17B of the cystic fibrosis transmembrane conductance regulator (CFTR) gene N. MorralE. GirbauX. Estivill OriginalPaper Pages: 356 - 356
A possible example of gene conversion with a common β-thalassemia mutation and Chi sequence present in the β-globin gene Youko MatsunoYasuhiro YamashiroTakaoki Miyaji Letters to the Editors Pages: 357 - 358
Germinal “mosaicism” — germline mutation or chimerism? Regine Witkowski Letters to the Editors Pages: 359 - 360
Prader-Willi or Angelman syndrome in familial 15q11→q13 deletion of maternal origin? Albert SchinzelWendy P. RobinsonAndrea Prader Letters to the Editors Pages: 361 - 362
High population incidence of the 15p marker D15Z1 mapping to the short arm of one homologue 14 K. StergianouC. P. GouldM. Hultén Letters to the Editors Pages: 364 - 364
Chromosome 15p marker D15Z1 frequently maps to the short arm of other D-group chromosomes Dominique F. C. M. SmeetsGerard F. M. MerkxAnton H. M. Hopman Letters to the Editors Pages: 365 - 365
