Selection of DNA sequences from interval 6 of the human Y chromosome with homology to a Y chromosomal fertility gene sequence of Drosophila hydei P. VogtR. KeilG. Lewe Original Investigations Pages: 341 - 349
Chromosome assignment of four RAS-related RAB genes Marie-Françoise Rousseau-MerckAhmed ZahraouiRoland Berger Original Investigations Pages: 350 - 354
Spectrum of phenylketonuria mutations in Western Europe and North Africa, and their relation to polymorphic DNA haplotypes at the phenylalanine hydroxylase locus Monique BerthelonCatherine CaillaudStanislas Lyonnet Original Investigations Pages: 355 - 358
Duplication of exons 13, 14 and 15 of the LDL-receptor gene in a patient with heterozygous familial hypercholesterolemia N. LelliM. GhiselliniS. Bertolini Original Investigations Pages: 359 - 362
A diallelic RFLP of the CD3-epsilon chain of the clonotypic T-lymphocyte receptor is not associated with certain autoimmune diseases Marcos TimónAntonio Arnaiz-VillenaJosé R. Regueiro Original Investigations Pages: 363 - 364
A new deletion polymorphism at D5S71 raises the linkage information on adenomatous polyposis coli: implications for presymptomatic diagnosis C. M. J. TopsC. BreukelP. Meera Khan Original Investigations Pages: 365 - 368
Characterization of a frequent polymorphism in the coding sequence of the Tp53 gene in colonic cancer patients and a control population Sylviane OlschwangPierre Laurent-PuigGilles Thomas Original Investigations Pages: 369 - 370
Some Mexican glucose-6-phosphate dehydrogenase variants revisited Ernest BeutlerWanda KuhlRuben Lisker Original Investigations Pages: 371 - 374
A molecular genetic approach to the identification of isochromosomes of chromosome 21 Lisa G. ShafferColleen K. Jackson-CookJ. Edward Spence Original Investigations Pages: 375 - 382
Predivision in human oocytes at meiosis I: a mechanism for trisomy formation in man Roslyn R. Angell Original Investigations Pages: 383 - 387
Mapping the gene encoding the human erythroid transcriptional factor NFE1-GF1 to Xp11.23 A. CaiuloS. NicolisB. Giglioni Original Investigations Pages: 388 - 390
Identification of a cystic fibros is mutation: deletion of isoleucine506 Paul V. NelsonWilliam F. CareyC. Phillip Morris Original Investigations Pages: 391 - 393
A novel human multi-locus DNA family detected by pJU78 (DF31) Frank PeinemannDavid N. CooperJörg Schmidtke Original Investigations Pages: 394 - 397
Localization of the human Rh blood group gene structure to chromosome region 1p34.3–1p36.1 by in situ hybridization B. Chérif-ZaharM. G. MattéiY. Colin Original Investigations Pages: 398 - 400
No evidence for sequences structurally related to the RB1 gene in the human genome Claus BelkaValerie GregerBernhard Horsthemke Original Investigations Pages: 401 - 403
Linkage analysis in X-linked adrenoleukodystrophy and application in post-and prenatal diagnosis B. A. van OostP. M. van ZandvoortH. H. Ropers Original Investigations Pages: 404 - 407
Geographical distribution gradients of the major PKU mutations and the linked haplotypes L. KalaydjievaB. DworniczakJ. Horst Short Communications Pages: 411 - 413
Characterisation of a Xp21 microdeletion syndrome in a 2-year-old boy with muscular dystrophy, glycerol kinase deficiency and adrenal hypoplasia congenita M. StuhrmannH. HeilbronnerJ. Schmidtke Short Communications Pages: 414 - 415
Homozygous condition for a BrdU-requiring fragile site on chromosome 12 I. VoiculescuE. BackW. Schempp Short Communications Pages: 416 - 417
Physical mapping of two Xp markers DXS16 and DXS143 Ulrike ThiesV. V. N. Gopal RaoJörg Schmidtke Short Communications Pages: 418 - 420
De novo complex chromosomal rearrangement in a woman with recurrent spontaneous abortion and one healthy daughter László TimárJudit BéresIrén Németh Case Observed Pages: 421 - 421
Probe KK5.33 (D5S85) improves indirect genotype analysis in familial adenomatous polyposis W. FriedlA. KrömerP. Propping Letter to the Editors Pages: 422 - 423
