Diagnosis of genetic disease using recombinant DNA. Third edition D. N. CooperJ. Schmidtke Review Article Pages: 519 - 560
Possible mapping of the gene for transient myeloproliferative syndrome at 21q11.2 Norio NiikawaHan-Xiang DengTadashi Kajii Original Investigations Pages: 561 - 566
Increased SOD1 enzymatic activity and gene modifications in orangutans: evolutionary implications Jean de GrouchyAnnie NicoleNicole Créau-Goldberg Original Investigations Pages: 567 - 570
Studies on the phylogenetic conservation of the SRY gene Terrence R. TierschMichael J. MitchellStephen S. Wachtel Original Investigations Pages: 571 - 573
Polymorphisms of the gene encoding cholesterol ester transfer protein and serum lipoprotein levels in subjects with and without coronary heart disease Heli TenkanenPekka KoskinenChristian Ehnholm Original Investigations Pages: 574 - 578
A 5′-truncated c-myc gene variant not associated with a risk of cancer N. S. PellegataG. BergamaschiG. N. Ranzani Original Investigations Pages: 579 - 582
“Spontaneous” FRA16B is a hot spot for sister chromatid exchanges T. LukusaE. MeulepasJ. J. Cassiman Original Investigations Pages: 583 - 586
Two unrelated children with partial trisomy 1q and monosomy 6p, presenting with the phenotype of the Larsen syndrome G. PierquinN. Van RegemorterE. Vamos Original Investigations Pages: 587 - 591
Synthesis of glycosaminoglycans in fibroblasts from abortuses with trisomy, triploidy, and from children with Down's syndrome V. I. KukharenkoE. M. PichuginaA. A. Delvig Original Investigations Pages: 592 - 596
Nucleotide sequence evidence of the unicentric origin of the βC mutation in Africa Guy TrabuchetJacques ElionDominique Labie Original Investigations Pages: 597 - 601
Analysis of synaptonemal complexes in a heterozygous human male carrier of a reciprocal translocation involving an acrocentric chromosome: heterosynapsis without previous homosynapsis A. de PerdigoO. Gabriel-RobezY. Rumpler Original Investigations Pages: 602 - 606
The molecular genetics of haemophilia A: screening for point mutations in the factor VIII gene using the restriction enzyme TaqI David S. MillarBarbara ZollDavid N. Cooper Original Investigations Pages: 607 - 612
Methods for analysis of multiple cystic fibrosis mutations Ivy S. L. NgRobert PaceArthur L. Beaudet Original Investigations Pages: 613 - 617
Chromosomal localization of the human D3 dopamine receptor gene Maryvonne Le ConiatPierre SokoloffRoland Berger Short Communications Pages: 618 - 620
Regional assignment of the human cell cycle control gene CDC2 to chromosome 10q21 by in situ hybridization S. A. NazarenkoN. V. OstroverhovaN. K. Spurr Short Comunications Pages: 621 - 622
The gene for the type II (p75) tumor necrosis factor receptor (TNF-RII) is localized on band 1p36.2–p36.3 Oliver KemperJosette DerréRoland Berger Short Comunications Pages: 623 - 624
Localisation of the gene coding for the haemopoietic stem cell antigen CD34 to chromosome 1q32 Spencer M. HowellHarald V. MolgaardNigel K. Spurr Short Comunications Pages: 625 - 627
Glutathione S-transferase class μ in French alcoholic cirrhotic patients Alexis GroppiChristiane CoutellePatrice Couzigou Short Comunications Pages: 628 - 630
An unusual variant detected using a β-globin probe for an individual with the sickle cell trait Rohan TaylorM. PattonS. Jeffery OriginalPaper Pages: 631 - 631
DNA-fingerprinting: a short note on mutation rates Michael KrawczakBarbara Bockel Letters to the Editors Pages: 632 - 633
Segregation of lymphocyte low molecular weight DNA and antinuclear antibodies in a family with systemic lupus erythematosus in first cousins M. A. FletcherP. PhillipsP. J. Benke OriginalPaper Pages: 634 - 634