Development of a sequence-tagged site for the centromere of chromosome 10: its use in cytogenetic and physical mapping James R. HoweTerry C. LairmoreHelen Donis-Keller Original Investigations Pages: 199 - 204
Detection of a cryptic paracentric inversion within band 11p13 in familial aniridia by fluorescence in situ hybridization Yoshimitsu FukushimaJan HooversNorio Niikawa Original Investigations Pages: 205 - 209
Deletion of 19 base pairs in intron 13 of the gene for the proα2(I) chain of type-I procollagen (COL1A2) causes exon skipping in a proband with type-I osteogenesis imperfecta Jiapiao ZhuangGerard TrompDarwin J. Prockop Original Investigations Pages: 210 - 216
Chromosomal localization of four human zinc finger cDNAs Kay HuebnerTeresa DruckLuigi Lania Original Investigations Pages: 217 - 222
Genetic epidemiology of sensorimotor polyneuropathy with or without agenesis of the corpus callosum in northeastern Quebec M. De BraekeleerA. DallaireJ. Mathieu Original Investigations Pages: 223 - 227
Human reciprocal translocations: is the unbalanced mode at birth predictable? Christine CansOlivier CohenPierre Jalbert Original Investigations Pages: 228 - 232
A novel mutation in exon 3 of the CFTR gene H. GuillermitM. JéhanneC. Férec Original Investigations Pages: 233 - 235
Steroid 21-hydroxylase (P450c21): a new allele and spread of mutations through the pseudogene Anna WedellHolger Luthman Original Investigations Pages: 236 - 240
Nucleotide substitutions at the -6 position in the promoter region of the factor IX gene result in different severity of hemophilia B Leyden: consequences for genetic counseling Dominique VidaudMichel TartaryMichel Vidaud Original Investigations Pages: 241 - 244
Partial physical map of human chromosome 21 from fibroblast and lymphocyte DNA Nathalie CrétéJean-Maurice DelabarNicole Créau-Goldberg Original Investigations Pages: 245 - 253
Analysis of 160 CF chromosomes: detection of a novel mutation in exon 20 I. DorvalS. OdentM. Blayau Original Investigations Pages: 254 - 256
Colocalization of the genes coding for the α3 and β3 subunits of soluble guanylyl cyclase to human chromosome 4 at q31.3–q33 Galicia GiuiliNathalie RoechelGeorges Guellaen Original Investigations Pages: 257 - 260
The immunoglobulin κ locus: polymorphism and haplotypes of Caucasoid and non-Caucasoid individuals Gudrun SchaibleGudrun A. RappoldHans G. Zachau Original Investigations Pages: 261 - 267
The effect of the apolipoprotein E phenotype on plasma lipids is not influenced by environmental variability: results of a Dutch twin study Peter de KnijffDorret I. BoomsmaLouis M. Havekes Original Investigations Pages: 268 - 272
A recombinant Friedreich's ataxia family G. LucotteS. BerricheJ. C. Turpin Short Communications Pages: 273 - 274
The 11p15.5 ribonucleotide reductase M1 subunit locus is not imprinted in Wilms' tumour and hepatoblastoma Jennifer A. ByrnePeter J. Smith Short Communications Pages: 275 - 277
Chrosomal mapping of the human gene for the tricyclic antidepressant-sensitive noradrenaline transporter Michael BrüssJürgen KunzHeinz Bönisch Short Communications Pages: 278 - 280
Parathyroid hormone gene analysis in autosomal hypoparathyroidism using an intragenic tetranucleotide (AAAT) n polymorphism D. B. ParkinsonN. J. ShawR. V. Thakker Short Communications Pages: 281 - 284
Distinct molecular origins for Denys-Drash and Frasier syndromes F. PoulatD. MorinP. Berta Short Communications Pages: 285 - 286
Identification of the 408 valine to methionine mutation in the low density lipoprotein receptor in a German family with familial hypercholesterolemia H. SchusterH. J. FischerN. Zöllner Short Communications Pages: 287 - 289
Polymorphism of glucose dehydrogenase (GDH, EC 1.1.1.47): formal and population genetic data D. KrczalH. RitterJ. Kömpf Short Communications Pages: 290 - 292
G6PD Mediterranean accounts for the high prevalence of G6PD deficiency in Kurdish Jews Ariella OppenheimCorrine L. JuryLucio Luzzatto Short Communications Pages: 293 - 294
Epidemiological data on Werdnig-Hoffmann disease in Germany (West-Thüringen) Andrea ThiemeBeate MitullaAribert W. J. Spiegier Short Communications Pages: 295 - 297
An interleukin-8 (IL-8) cDNA clone identifies a frequent HindIII polymorphism M. F. FeyA. Tobler DNA Variants Pages: 298 - 298
Absence of familial defective apolipoprotein B-100 in Israeli patients with dominantly inherited hypercholesterolemia and in offspring with parental history of myocardial infarction Yechiel FriedlanderEldad J. DannEran Leitersdorf Letters to the Editors Pages: 299 - 300
The relationship between meiotic chromosome pairing and chiasma formation Maj HulténAlastair Goldman Letters to the Editors Pages: 300 - 300
Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fcγ receptor gene region Roger V. LeboPhillip F. ChanceP. Michael Conneally Erratum Pages: 301 - 301
