The polymerase chain reaction: an improved method for the analysis of nucleic acids Hans-Peter Vosberg Review Articles Pages: 1 - 15
Prenatal diagnosis of genetic disorders in preimplantation embryos: invasive and non-invasive approaches Matteo AdinolfiPaul E. Polani Review Articles Pages: 16 - 19
Cystic fibrosis in Finland: a molecular and genealogical study Juha KereReijo NorioAlbert de la Chapelle Original Investigations Pages: 20 - 25
How does inactivation change timing of replication in the human X chromosome? Sabine SchwemmleKarl MehnertWalther Vogel Original Investigations Pages: 26 - 32
Assignment of human desmin gene to band 2q35 by nonradioactive in situ hybridization Evani Viegas-PéquignotLi Zhen LinDenise Paulin Original Investigations Pages: 33 - 36
BamHI and SacI RFLPs of the human immunoglobulin IGHG genes with reference to the Gm polymorphism in African people N. GhanemM. BensmanaG. Lefranc Original Investigations Pages: 37 - 44
Fibroblast-specific common fragile sites induced by aphidicolin I. MuranoA. KuwanoT. Kajii Original Investigations Pages: 45 - 48
Partial correction of chromosome instability in Fanconi anemia by desferrioxamine B. PorfirioG. AmbrosoB. Dallapiccola Original Investigations Pages: 49 - 51
Risks of fetal cystic fibrosis based on linkage disequilibrium data Susan HollowayD. J. H. Brock Original Investigations Pages: 52 - 54
Autosomal dominant polycystic kidney disease and α−4.2 thalassemia in a Caucasian family Marie Claude VinetCatherine DodéLucien Bachner Original Investigations Pages: 55 - 57
Selection of human chromosome 21-specific DNA probes for genetic analysis in Alzheimer's dementia and Down syndrome Guy Van CampPiet StinissenChristine Van Broeckhoven Original Investigations Pages: 58 - 60
Assignment of anonymous DNA probes to specific intervals of human chromosomes 16 and X V. J. HylandK. E. W. FernandezG. R. Sutherland Original Investigations Pages: 61 - 66
Multiple mutations underlying familial hypercholesterolemia in the South African population Howard E. HendersonMaritha J. KotzeG. Michael B. Berger Original Investigations Pages: 67 - 70
Long-range restriction map of a region of human chromosome 19 containing the apolipoprotein genes, a CLL-associated translocation breakpoint, and two polymorphic MluI sites Duncan J. ShawHelen G. HarleyTimothy W. McKeithan Original Investigations Pages: 71 - 74
A novel δ° arising from a frameshift insertion, detected by direct sequencing of enzymatically amplified DNA Monique LosekootRiccardo FoddeLuigi F. Bernini Original Investigations Pages: 75 - 78
Cytogenetic investigations in a family with ataxia telangiectasia M. W. HumphreysN. C. NevinM. A. W. Wooldridge Original Investigations Pages: 79 - 82
Detection of an unbalanced translocation (4;14) in a mildly retarded father and son by flow cytometry Alexander CookeJohn L. TolmieJ. Michael Connor Original Investigations Pages: 83 - 87
Molecular analysis of 46,XY females and regional assignment of a new Y-chromosome-specific probe Michael A. CantrellJames N. BicknellChristine M. Disteche Original Investigations Pages: 88 - 92
Detection of an alteration of the α2 gene in a patient with chronic lung disease and serum α2 deficiency W. PollerJ. BarthB. Voss Short Communications Pages: 93 - 96
Linkage analyses of human peptidase C (PEPC), human factor H (HF), and coagulation factor XIIIB (F13B) J. KömpfC. LuckenbachH. Ritter Short Communications Pages: 97 - 98