Diagnosis of genetic disease using recombinant DNA. Second edition D. N. CooperJ. Schmidtke Review Article Pages: 307 - 334
The gene encoding human low-molecular weight insulin-like growth-factor binding protein (IGF-BP25): regional localization to 7p12–p13 and description of a DNA polymorphism Tiina AlitaloKimmo KontulaAlbert de la Chapelle Original Investigations Pages: 335 - 338
Clinical and biochemical studies in three patients with severe early infantile Cockayne syndrome Jaak JackenHelmut KlockerManfred Schweiger Original Investigations Pages: 339 - 346
Tissue specificity of chromosomal rearrangements in ataxia-telangiectasia T. L. KojisR. R. SchreckR. S. Sparkes Original Investigations Pages: 347 - 352
Linkage analysis of hereditary thyroid carcinoma with and without pheochromocytoma Steven A. NarodHagay SobolGilbert M. Lenoir Original Investigations Pages: 353 - 358
Molecular analysis of the isochromosome 12P in the Pallister-Killian syndrome Ji ZhangPeter MarynenJean-Jacques Cassiman Original Investigations Pages: 359 - 363
Apolipoprotein (apo) E genotypes by polymerase chain reaction and allele-specific oligonucleotide probes: no detectable linkage disequilibrium between apo E and apo CII R. S. HoulstonC. SnowdenS. E. Humphries Original Investigations Pages: 364 - 368
Haplotype frequencies of the collagen type-I genes in the Italian population Monica MottesLoredana CugolaPier Franco Pignatti Original Investigations Pages: 369 - 372
Two distinct variants of erythrocyte spectrin βIV domain B. PothierN. AlloisioJ. Delaunay Original Investigations Pages: 373 - 376
Deletion/frameshift mutation in the α1 null allele, PI*QObolton Gail C. FraizerMonica SiewertsenDiane W. Cox Original Investigations Pages: 377 - 382
The β subunit locus of the human fibronectin receptor: DNA restriction fragment length polymorphism and linkage mapping studies Jingshi WuLuis A. GiuffraKenneth K. Kidd Original Investigations Pages: 383 - 390
Linkage disequilibrium and CF allele segregation analysis in cystic fibrosis families in Northern Ireland Alison J. M. HillColin A. GrahamNorman C. Nevin Original Investigations Pages: 391 - 394
TaqI polymorphism within the c-Ha-ras-1 VTR is associated with melanoma N. K. HaywardD. J. NancarrowK. A. O. Ellem Letter to the Editors Pages: 395 - 396