In situ hybridization localizes the human putative oncogene GLI to chromosome subbands 12q13.3–14.1 Kristina ArhedenMogens RønneFelix Mitelman Original Investigations Pages: 1 - 2
Population cytogenetics of folate-sensitive fragile sites M. KähkönenC. TengströmE. Airaksinen Original Investigations Pages: 3 - 8
Haplotype analysis of familial amyloidotic polyneuropathy Katsuji YoshiokaHirokazu FuruyaYoshiyuki Sakaki Original Investigations Pages: 9 - 13
Genotypes of alcohol dehydrogenase and aldehyde dehydrogenase loci in Japanese alcohol flushers and nonflushers Akitaka ShibuyaMichio YasunamiAkira Yoshida Original Investigations Pages: 14 - 16
Regional assignment of the loci for adenylate kinase to 9q32 and for α1-acid glycoprotein to 9q31-q32 Orsetta ZuffardiAngela CaiuloG. Liguri Original Investigations Pages: 17 - 19
Parental age and the origin of trisomy 21 F. Dagna BricarelliM. PierluigiP. Strigini Original Investigations Pages: 20 - 26
Physical mapping of DXS134 close to the DXS52 locus M. V. BellM. N. PattersonK. E. Davies Original Investigations Pages: 27 - 30
Cytogenetic and in situ DNA-hybridization studies in intracranial tumors of a patient with central neurofibromatosis B. WullichM. Kiechle-SchwarzW. Schempp Original Investigations Pages: 31 - 34
Differential associative behaviour of mitotic and meiotic acrocentric chromosomes M. C. DumontM. J. BelloJ. M. Luciani Original Investigations Pages: 35 - 39
Mapping of the gene encoding the multifunctional protein carrying out the first three steps of pyrimidine biosynthesis to human chromosome 2 Kuey-Chu ChenDiane B. VannaisJeffrey N. Davidson Original Investigations Pages: 40 - 44
Pseudodeficiency of arylsulfatase A: a common genetic polymorphism with possible disease implications Charlotte HohenschutzPeter EichPeter Propping Original Investigations Pages: 45 - 48
The absence of type II collagen and changes in proteoglycan structure of hyaline cartilage in a case of Langer-Saldino achondrogenesis S. P. FeshchenkoI. A. RebrinG. I. Lazjuk Original Investigations Pages: 49 - 54
DNA restriction fragment length polymorphisms in differential diagnosis of genetic disease: application in neuromuscular diseases J. C. DefescheM. de VisserP. A. Bolhuis Original Investigations Pages: 55 - 58
Non C-banding variants in some normal families might be homogeneously staining regions Graham C. WebbEdgar J. M. KruminsKong H. Choo Original Investigations Pages: 59 - 62
Heterogeneity of mRNA expression in Italian fucosidosis patients S. GuazziP. PersiciG. Romeo Original Investigations Pages: 63 - 66
Chromosomal localization of ARSB, the gene for human N-acetylgalactosamine-4-sulphatase Tom LitjensElizabeth G. BakerDavid F. Callen Original Investigations Pages: 67 - 68
Four DNA polymorphisms in the LDL-receptor gene and their use in diagnosis of familial hypercholesterolemia H. SchusterB. StiefenhoferN. Zöllner Original Investigations Pages: 69 - 72
Genetics of the quantitative Lp(a) lipoprotein trait Eric BoerwinkleHans Jürgen MenzelGerd Utermann Original Investigations Pages: 73 - 78
The role of recombination in the evolvement of the fragile X mutation Tamar Schaap Original Investigations Pages: 79 - 81
Mapping the human ZFX locus to Xp21.3 by in situ hybridization Gaby MüllerWerner Schempp Short Communications Pages: 82 - 84
A new polymorphic marker very closely linked to DXS52 in the q28 region of the human X chromosome A. VincentC. KretzJ. L. Mandel Short Communications Pages: 85 - 86
Localization of human platelet proteoglycan gene to chromosome 10, band q22.1, by in situ hybridization M. G. MatteiJ. -P. PérinP. Jollès Short Communications Pages: 87 - 88
A hereditary double double-banded variation in the vitamin D-binding protein (GC) system analyzed by immunoblotting: duplication of the 1F and 1A2 genes? Toshihiro YasudaYoko IkeharaKoichiro Kishi Short Communications Pages: 89 - 91
Unbalanced translocation between chromosomes 2 and 7 with de novo deletion of band 35 on the long arm of chromosme 2 P. E. LundbechT. Thøgersen Clinical Case Report Pages: 92 - 93
PLG A91 and PLG M6: two new plasminogen allotypes in Japan I. YuasaK. SuenagaK. Okada Rare Genetic Variant Register Pages: 94 - 94
EcoRI RFLP in the human thyroid peroxidase (TPO) gene on chromosome 2 H. BikkerP. A. BolhuisJ. J. M. de Vijlder DNA Variants Pages: 95 - 95
Remarks on the article “Use of linkage equilibrium data in prenatal diagnosis of cystic fibrosis” by L. Strain et al. Gerard J. te MeermanCharles H. C. M. Buys Letters to the Editors Pages: 96 - 97
Response to Wiberg's remarks on our article: “H-Y antigenicity of human fibroblasts” C. JorgensenE. J. Eichwald Letters to the Editors Pages: 98 - 98