The Kidd (JK) blood group locus assigned to chromosome 18 by close linkage to a DNA-RFLP G. A. GeitvikB. HøyheimB. Olaisen Original Investigations Pages: 205 - 209
Do individual allocyclic chromosomes in metaphase reflect their interphase domains? Evelyn M. KuhnEeva ThermanDolores A. Buchler Original Investigations Pages: 210 - 213
Gene-rich chromosome regions and autosomal trisomy Evelyn M. KuhnGloria E. SartoEeva Therman Original Investigations Pages: 214 - 220
Autosomal recessive and dominant forms of polycystic kidney disease are not allelic Brunhilde WirthK. ZerresA. Gal Original Investigations Pages: 221 - 222
Development of the first meiotic prophase stages in human fetal oocytes observed by light and electron microscopy M. GarciaA. J. J. DietrichJ. Egozcue Original Investigations Pages: 223 - 232
Linkage relationships of X-linked choroideremia to DXYS1 and DXS3 I. M. MacDonaldR. M. SandreM. P. R. Tenniswood Original Investigations Pages: 233 - 235
Determining the origin of human X isochromosomes by use of DNA sequence polymorphisms and detection of an apparent i(Xq) with Xp sequences David F. CallenJohn C. MulleyGrant R. Sutherland Original Investigations Pages: 236 - 240
Functional hemizygosity in the human genome: direct estimate from twelve erythrocyte enzyme loci H. W. Mohrenweiser Original Investigations Pages: 241 - 245
Pachytene analysis in a 17;21 reciprocal translocation carrier: role of the acrocentric chromosomes in male sterility J. M. LucianiM. R. GuichaouaY. Rumpler Original Investigations Pages: 246 - 250
Chromosomal insertion of human papillomavirus 18 sequences in HeLa cells detected by nonisotopic in situ hybridization and reflection contrast microscopy P. F. AmbrosH. I. Karlic Original Investigations Pages: 251 - 254
Orosomucoid (ORM) typing by isoelectric focusing: evidence for gene duplication of ORM1 and genetic polymorphism of ORM2 I. YuasaK. SuenagaM. Robinet-Levy Original Investigations Pages: 255 - 258
Genes for two homologous G-protein α subunits map to different human chromosomes Eva J. NeerThomas MichelJ. G. Seidman Original Investigations Pages: 259 - 262
Anderson Fabry disease, a close linkage with highly polymorphic DNA markers DXS17, DXS87 and DXS88 K. D. MacDermotS. H. MorganT. M. Wilson Original Investigations Pages: 263 - 266
Familial deletion in Becker type muscular dystrophy within the pXJ region Sabina Liechti-GallatiSuzanne BragaHans Moser Original Investigations Pages: 267 - 268
Loss of heterozygosity in hypotriploid cell cultures from testicular tumours Jennifer M. ParringtonLynne F. WestSusan Povey Original Investigations Pages: 269 - 276
Linkage relationship between the genes for adenosine deaminase and S-adenosyl-homocysteine hydrolase on human chromosome 20 S. BissbortH. W. HitzerothT. F. Wienker Original Investigations Pages: 277 - 279
Localization of the human progesterone receptor gene to chromosome 11q22–q23 M. F. Rousseau-MerckM. MisrahiR. Berger Original Investigations Pages: 280 - 282
Chromosomal assignment of the human 2,3-bisphosphoglycerate mutase gene (BPGM) to region 7q34→7q22 Fernande BarichardVirginie JoulinClaudine Junien Original Investigations Pages: 283 - 285
Three new orosomucoid (ORM) variants revealed by isoelectric focusing and print immunofixation S. WeidingerT. MüllerH. Cleve Short Communication Pages: 286 - 288
A case of Shwachman syndrome with increased spontaneous chromosome breakage H. TadaT. RiT. Shinohara Clinical Case Reports Pages: 289 - 291
Interstitial deletion of chromosome 13 involving the region 13q14 R. PankauW. JohannsonM. Tolksdorf Clinical Case Reports Pages: 292 - 293
An azoospermic male with reciprocal translocation t(1;15)(q11;p11) C. López-GinésR. GilA. Pellin Cases Observed Pages: 294 - 294
A new BF F variant by polyacrylamide gel isoelectric focusing S. NakamuraO. OhueK. Abe Genetic Variant Register Pages: 295 - 296
Interpretation of the heterogeneity in the linkage relationships of DNA markers around the fragile X locus Robin WinterMarcus Pembrey Letter to the Editors Pages: 297 - 298
