Increased satellite association induced by 5′ Bromodeoxyuridine treatment of Phytohemaglutinin-stimulated blood lymphocytes Jana MusilováKyra MichalováHelena Hoffmanová Original Investigations Pages: 91 - 93
Cystic fibrosis in the Ohio Amish: Gene frequency and founder effect Katherine Wood Klinger Original Investigations Pages: 94 - 98
Effect of oxygen tension on chromosomal aberrations in Fanconi anaemia H. JoenjeB. Oostra Original Investigations Pages: 99 - 101
A deficiency mutant of the Gc system B. VavrusaH. CleveJ. Constans Original Investigations Pages: 102 - 107
Interferon induction of (2′–5′) oligoisoadenylate synthetase in diploid and trisomy 21 human fibroblasts: Relation to dosage of the interferon receptor gene (IRFC) J. WeilGeorgianne TuckerC. J. Epstein Original Investigations Pages: 108 - 111
Complementation analysis in Gaucher disease using single cell microassay techniques. Evidence for a single “Gaucher gene” R. A. GravelA. Leung Original Investigations Pages: 112 - 116
A dominantly inherited cytogenetic anomaly: A possible cell division mutant Noreen L. RuddIluko E. TeshimaRosanna Weksberg Original Investigations Pages: 117 - 121
Familial, EsD-linked, retinoblastoma with reduced penetrance and variable expressivity M. J. ConnollyR. H. PayneR. D. Lawton Original Investigations Pages: 122 - 124
Are bowing of long tubular bones and preaxial polydactyly signs of the Meckel syndrome? F. MajewskiH. StößH. Kemperdick Original Investigations Pages: 125 - 133
Interstitial deletion for a region in the long arm of chromosome 16 C. C. LinR. B. LowryF. F. Snyder Original Investigations Pages: 134 - 138
The sequence of DNA replication in an iso-dicentric X-chromosome in peripheral blood lymphocytes and skin fibroblasts from the same individual M. S. LinM. G. Wilson Original Investigations Pages: 139 - 143
Methyl green is a substitute for distamycin A in the formation of distamycin A/DAPI C-bands T. A. DonlonR. E. Magenis Original Investigations Pages: 144 - 146
Glutamate pyruvate transaminase null allele in seven new families Maryellen C. SparkesM. CristR. S. Sparkes Original Investigations Pages: 147 - 148
Juvenile idiopathic haemochromatosis: A life-threatening disorder presenting as hypogonadotropic hypogonadism M. CazzolaE. AscariE. E. Werner Original Investigations Pages: 149 - 154
The genetic significance of accessory bisatellited marker chromosomes P. SteinbachM. DjalaliM. Wolf Original Investigations Pages: 155 - 164
Mating between two balanced translocation carriers in two unrelated families B. DallapiccolaL. ChessaE. Gandini Original Investigations Pages: 165 - 168
Genetic linkage relationships between the Xg blood group system and two X chromosome DNA polymorphisms in families with Duchenne and Becker muscular dystrophy M. SarfaraziP. S. HarperR. Sanger Original Investigations Pages: 169 - 171
Prenatal diagnosis of Tay-Sachs disease. Reflectometry of hexosaminidase A, B, and C/S bands on zymograms B. Kustermann-KuhnK. Harzer Original Investigations Pages: 172 - 175
The polymorphism of the vitamin D-binding protein (Gc); Isoelectric focusing in 3 M urea as additional method for identification of genetic variants J. ConstansH. CleveW. Weber Original Investigations Pages: 176 - 180
A genetic component of the variance of N-acetoxy-2-acetylaminofluorene-induced DNA damage in mononuclear leukocytes determined by a twin study R. W. PeroC. BryngelssonÅ. Nordén Original Investigations Pages: 181 - 184
Meiotic studies in a series of 1100 infertile and sterile males J. EgozcueC. TempladoS. Marina Original Investigations Pages: 185 - 188
On the identity of arylsulphatase C and steroid sulphatase G. Burns Original Investigations Pages: 189 - 189
Protein A radio-assay of H-Y antigen on human leukocytes using mouse and rat antisera and monoclonal antibodies H. SavikukiL. C. AnderssonA. de la Chapelle Original Investigations Pages: 190 - 194
Chromosomal localization of a human myosin heavy-chain gene by in situ hybridization Gudrun A. RappoldH.-P. Vosberg Original Investigations Pages: 195 - 197
Characterization of a human genomic DNA fragment coding for a myosin heavy chain H. AppelhansH.-P. Vosberg Original Investigations Pages: 198 - 203
Four new haplotypes observed in Algerian β-thalassemia patients C. BeldjordClaudine LapouméroulieD. Labie Original Investigations Pages: 204 - 206
Regional localization of the human factor IX gene by molecular hybridization P. F. ChanceKaren A. DyerS. M. Gartler Short Communications Pages: 207 - 208
Sex vesicle loss: A possible explanation of the excess of XO over XXY conceptuses in mice and men T. Ashley Short Communications Pages: 209 - 210
Fragile chromosome 16(q22) cause a balanced translocation at the same point J. M. García-SagredoC. San RománG. Lledo Clinical Case Reports Pages: 211 - 213
G6PD Sendagi: A new glucose-6-phosphate dehydrogenase variant associated with congenital hemolytic anemia T. MorisakiH. FujiiS. Miwa Clinical Case Reports Pages: 214 - 215
Inherited pericentric inversion of human chromosome 5 Giusi BarbataGiuseppina GranataPaolo Carbone Cases Observed Pages: 216 - 216
Inducible fragile site on chromosome 3 A. MarkkanenS. KnuutilaA. de la Chapelle Letters to the Editors Pages: 217 - 217
Reply to the letter of A. Markkanen, S. Knuutila, and A. de la Chapelle Rolf-Dieter Wegner Letters to the Editors Pages: 218 - 218
