Heterozygosity and ethnic variation in Japanese platelet proteins Jun-ichi AsakawaJames V. NeelMikio Fujita Original Investigations Pages: 1 - 8
A disease with features of cutis laxa and Ehlers-Danlos syndrome Masato TsukaharaHiroshi ShinkaiTadashi Kajii Original Investigations Pages: 9 - 12
β-thalassemia mutations in the Portuguese population M. P. Coutinho GomesM. G. Gomes da CostaA. Cao Original Investigations Pages: 13 - 15
Genetic transferrin types and iron-binding: a comparative study of a European and an African population sample H. CleveE. SchwendnerA. Bidlingmaier Original Investigations Pages: 16 - 20
Fragile sites induced by FUdR, caffeine, and aphidicolin P. Nagesh RaoNyla A. HeeremaCatherine G. Palmer Original Investigations Pages: 21 - 26
Organization and genomic distribution of “82H” alpha satellite DNA John S. WayeArthur R. MitchellHuntington F. Willard Original Investigations Pages: 27 - 32
Molecular characterization of different ataxia telangiectasia T-cell clones Marc-Henri SternFangrong ZhangAlain Aurias Original Investigations Pages: 33 - 36
Molecular basis of β thalassemia in South China Ji-Zeng ZhangShi-Ping CaiYuet Wai Kan Original Investigations Pages: 37 - 40
Genetics of the quantitative Lp(a) lipoprotein trait Gerd UtermannHans Georg KraftChristoph Seitz Original Investigations Pages: 41 - 46
Genetics of the quantitative Lp(a) lipoprotein trait Gerd UtermannChristoph DubaHans Jürgen Menzel Original Investigations Pages: 47 - 50
Fanconi's anaemia: correlation of genetic complementation group with psoralen/UVA response Martin DigweedSabine Zakrzewski-LüdckeKarl Sperling Original Investigations Pages: 51 - 54
A DNA polymorphism of an apoprotein gene associates with the hypertriglyceridaemia of primary gout G. A. A. FernsJ. LanhamD. J. Galton Original Investigations Pages: 55 - 59
Analysis of linkage relationships of X-linked retinitis pigmentosa with the following Xp loci: L1.28, OTC, 754, XJ-1.1, pERT87, and C7 Michael J. DentonJia-De ChenJennifer Donald Original Investigations Pages: 60 - 64
Assignment of the human fast skeletal muscle myosin alkali light chains gene (MLC1F/MLC3F) to 2q 32.1-2qter Odile Cohen-HaguenauerPaul J. R. BartonJean Frézal Original Investigations Pages: 65 - 70
Chromosomal radiosensitivity of Down syndrome lymphocytes at different stages of the cell cycle Hasnaa M. ShafikWilliam W. AuMarvin S. Legator Original Investigations Pages: 71 - 75
The Duffy blood group is linked to the α-spectrin locus in a large pedigree with autosomal dominant inheritance of Charcot-Marie-Tooth disease type 1 Peter RaeymaekersChristine Van BroeckhovenAntoon Vandenberghe Original Investigations Pages: 76 - 78
Genomic structure and evolution of the human pepsinogen A multigene family Bauke ZelleMarie Pauline J. EversRune R. Frants Original Investigations Pages: 79 - 82
Feto-maternal transfusion after chorionic villus sampling W. FuhrmannK. AltlandP. Miny Original Investigations Pages: 83 - 85
Alterations of class I HLA genes in human colon cancers Menashe Bar-EliHector BattiforaMartin J. Cline Original Investigations Pages: 86 - 89
Apolipoprotein gene cluster on chromosome 19 Marijke SmitEllien van der Kooij-MeijsEduard C. Klasen Short Communications Pages: 90 - 93
Localization of the spherocytosis gene to chromosome segment 8p11.22→8p21.1 M. KitataniH. ChiyoS. Miwa Short Communications Pages: 94 - 95
Assignment of the human progesterone receptor to the q22 band of chromosome 11 Marie-Geneviève MatteiAndrée KrustPierre Chambon Short Communications Pages: 96 - 97
G6PD Viangchan: a new glucose 6-phosphate dehydrogenase variant from Laos Man-Chiu PoonKelley HallJosef T. Prehal Short Communications Pages: 98 - 99
Absence of charge variants in human skeletal muscle enzymes of the glycolytic pathway Claude BouchardMonique ChagnonJean-Aimé Simonean Short Communications Pages: 100 - 100
Prevalence of the 281 (Gly→Glu) mutation in hepatoerythropoietic porphyria and porphyria cutanea tarda Hubert de VerneuilJoanna HansenYves Nordmann Short Communications Pages: 101 - 102
Multiple recurrence of trisomy 21 Down syndrome Kim Gjerum NielsenHanne PoulsenElke Steuber Clinical Case Report Pages: 103 - 105
Trichothiodystrophy, xeroderma pigmentosum and PIBI(D)S syndrome Alfredo ReboraFranco Crovato Letters to the Editors Pages: 106 - 108
BglII RFLPs in the COL1A2 gene in the Finnish population Raymond Dalgleish Letters to the Editors Pages: 109 - 109