The origin of cytologically unidentifiable chromosome abnormalities: six cases ascertained by targeted chromosome-band painting T. OhtaT. TohmaN. Niikawa Original Investigations Pages: 1 - 5
Screening for point mutations in exon 10 of the low density lipoprotein receptor gene by analysis of single-strand conformation polymorphisms: detection of a nonsense mutation — FH469→Stop Trond P. LerenKari SolbergKåre Berg Original Investigations Pages: 6 - 10
Rearrangements between irradiated chromosomes in three-species radiation hybrid cell lines revealed by two-color in situ hybridization C. PhilippeV. C. NguyenA. Bernheim Original Investigations Pages: 11 - 17
Physical mapping of chromosome 3p25-p26 by flourescence in situ hybridisation (FISH) M. E. PhippsE. R. MaherM. A. Ferguson-Smith Original Investigations Pages: 18 - 22
Presence of telomeric and subtelomeric sequences at the fusion points of ring chromosomes indicates that the ring syndrome is caused by ring instability Annalisa PezzoloGiorgio GimelliOrsetta Zuffardi Original Investigations Pages: 23 - 27
Meiotic recombination in an Irish family with beta-thalassaemia Georgina W. HallMaurizio SampietroSweeLay Thein Original Investigations Pages: 28 - 32
Altered CYP21 genes in HLA-haplotypes associated with congenital adrenal hyperplasia (CAH): a family study Burkhard J. ManfrasMichael SwinyardBernhard O. Böhm Original Investigations Pages: 33 - 39
Recurrent mutations in the factor IX gene: founder effect or repeat de novo events O. KnoblochB. ZollM. Ludwig Original Investigations Pages: 40 - 48
For novel gene mutations in five Japanese male patients with neonatal or late onset OTC deficiency: application of PCR-single-strand conformation polymorphisms for all exons and adjacent introns Toshinobu MatsuuraRyuuji HoshideIchiro Matsuda Original Investigations Pages: 49 - 56
No relationship between genetic instability in Bloom's syndrome and DNA hypomethylation of some major repetitive sequences P. NoguiezC. JaulinM. Amor-Gueret Original Investigations Pages: 57 - 60
G2 phase cell cycle disturbance as a manifestation of genetic cell damage Helga SeyschabYujie SunHolger Hoehn Original Investigations Pages: 61 - 68
The human complement component C8B gene: structure and phylogenetic relationship Thomas KaufmannChristian RittnerPeter M. Schneider Original Investigations Pages: 69 - 75
Four new nucleotide sequence polymorphisms in the LDL receptor gene detected by SSCP analysis Kimiko Yamakawa-KobayashiTsutomu KobayashiHideo Hamaguchi Short Communications Pages: 76 - 78
Alpha-thalassemia in the four major aboriginal groups in Taiwan Tsang-Ming KoTai-Ann ChenTzu-Yao Lee Short Communications Pages: 79 - 80
Genetic variation in transforming growth factor alpha: possible association of BamHI polymorphism with bilateral sporadic cleft lip and palate C. StollJ. F. QianE. May Short Communications Pages: 81 - 82
Insertional inactivation of the WT1 gene in tumour cells from a patient with WAGR syndrome Ana SantosLeonor Osorio-AlmeidaJohn Cowell Short Communications Pages: 83 - 86
Gene for hereditary neuropathy with liability to pressure palsies (HNPP) maps to chromosome 17 at or close to the locus for HMSN type 1 Edwin C. M. MarimanAnneke A. W. M. Gabreëls-FestenFons J. M. Gabreëls Short Communications Pages: 87 - 90
Absence of linkage to the ataxia telangiectasia locus in familial breast cancer Richard WoosterDeborah FordMichael R-Stratton Short Communications Pages: 91 - 94
Physical mapping shows close linkage between the α-galactosidase A gene (GLA) and the DXS178 locus David VetrieDavid BentleyAnn Harris Short Communications Pages: 95 - 99
PCR-based detection of one BamHI polymorphic site in the human T cell receptor delta gene TCRDV2 X. M. ZhangM. -P. Lefranc DNA Variants Pages: 100 - 100
High frequency of mutations at position 11778 in mitochondrial ND4 gene in Japanese families with Leber's hereditary optic neuropathy Yukihiko MashimaYoshiki HiidaNobuyoshi Shimizu DNA Variants Pages: 101 - 102
Identification of a novel T-insertion polymorphism at the DMD locus F. MuntoniM. CauM. A. Melis DNA Variants Pages: 103 - 103
Prothymosin α gene in humans: organization of its promoter region and localization to chromosome 2 P. SzaboC. PanneerselvamB. L. Horecker Errata Pages: 104 - 104
The immunoglobulin κ locus: polymorphism and haplotypes of Caucasoid and non-Caucasoid individuals Gudrun SchaibleGudrun A. RappoldHans G. Zachau Errata Pages: 105 - 105
