DNA polymorphism and molecular pathology of the human globin gene clusters Stylianos E. AntonarakisHaig H. Kazazian Jr.Stuart H. Orkin Review Articles Pages: 1 - 14
A new glucose-6-phosphate dehydrogenase variant, Gd(-) Tepic, characterized by moderate enzyme deficiency and mild episodes of hemolytic anemia Rubén LiskerRocio Pérez-BriceñoErnest Beutler Original Investigations Pages: 19 - 21
Clinical and cytogenetic studies of the Prader-Willi syndrome: Evidence of phenotype-karyotype correlation N. NiikawaS. Ishikiriyama Original Investigations Pages: 22 - 27
Localization of the thyroglobulin gene by in situ hybridization to human chromosomes Jean-Louis Bergé-LefrancGuy CartouzouSerge Lissitzky Original Investigations Pages: 28 - 31
Cotransfer of syntenic human genes into mouse cells using isolated metaphase chromosomes or cellular DNA A. J. R. de JongeS. de SmitA. J. J. Reuser Original Investigations Pages: 32 - 38
Linkage relationships of the gene for apolipoprotein CII with loci on chromosome 19 J. A. DonaldS. C. WallisS. E. Humphries Original Investigations Pages: 39 - 43
Linkage and recombination between fragile X-linked mental retardation and the factor IX gene Stephen T. WarrenThomas W. GloverPudur Jagadeeswaran Original Investigations Pages: 44 - 46
Maternal serum alpha-fetoprotein screening for neural tube defects Walter FuhrmannHans K. Weitzel Original Investigations Pages: 47 - 61
Effect of oxidants and antioxidants on chromosomal breakage in Fanconi anemia lymphocytes B. DallapiccolaB. PorfirioE. Gandini Original Investigations Pages: 62 - 65
The hereditary transmission of high glutathione transferase activity towards trans-stilbene oxide in human mononuclear leukocytes Janeric SeidegårdRonald W. Pero Original Investigations Pages: 66 - 68
The prophase stages in human foetal oocytes studied by light and electron microscopy R. M. Speed Original Investigations Pages: 69 - 75
Impaired insulin-induced RNA synthesis secondary to a genetically defective insulin receptor H. W. RüdigerP. AhrensU. Schmidt-Preuß Original Investigations Pages: 76 - 78
46,XY gonadal dysgenesis: Isoncogenesis related to H-Y phenotype or breast development? Barry A. WarnerRonald P. MonsaertStephen S. Wachtel Original Investigations Pages: 79 - 85
High resolution R banding in amniotic fluid cells using the BrdU-Hoechst 33258-Giemsa (RBG) technique Sau W. CheungJames P. CraneAnn C. Burgess Short Communications Pages: 86 - 87
Prenatal selection and fetal development disturbances occurring in carriers of G6PD deficiency D. TonchevaM. Tzoneva Short Communications Pages: 88 - 88
Gc subtypes identified by isoelectric focusing in Baboons (Papio hamadryas) Dale DykesMichael CrawfordHerbert Polesky Short Communications Pages: 89 - 90
Evidence of a preferential inactivation of the paternally derived X chromosome in a 46,XX true hermaphrodite C. BoucekkineD. NafaM. Benmiloud Short Communications Pages: 91 - 93
