Population structure of Sicily: beta-thalassemia and HbS Italo BarraiGino SchiliroGiovanna Russo Mancuso Original Investigations Pages: 1 - 3
A heritable fragile 12q24.13 segregating in a family with the fragile X chromosome Anthony P. AmarosePeter R. HuttenlocherMark J. Pettenati Original Investigations Pages: 4 - 6
Genetic analysis of febrile convulsions: twin and family studies T. Tsuboi Original Investigations Pages: 7 - 14
Deficiency of AMP deaminase in erythrocytes N. OgasawaraH. GotoK. S. Park Original Investigations Pages: 15 - 18
Detection of duchenne muscular dystrophy carriers: quantitative echography and creatine kinasemia Georges SchapiraPascal LaugierJean Perrin Original Investigations Pages: 19 - 23
Single cell translocations in couples with multiple spontaneous abortions Michael D. HigginsCatherine G. Palmer Original Investigations Pages: 24 - 27
Characterization of a series of electrophoretic and enzyme activity variants of human glucose-phosphate isomerase H. W. MohrenweiserP. T. WadeK. H. Wurzinger Original Investigations Pages: 28 - 31
Genetic linkage study between the loci for Duchenne and Becker muscular dystrophy and nine X-chromosomal DNA markers E. WilichowskiM. KrawczakJ. Schmidtke Original Investigations Pages: 32 - 40
The gene encoding vasoactive intestinal peptide is located on human chromosome 6p21→6qter Illana GozesRina AvidorKay Huebner Original Investigations Pages: 41 - 44
Two complementation groups of Fanconi's anemia differ in their phenotypic response to a DNA-crosslinking treatment E. MoustacchiD. PapadopouloM. Buchwald Original Investigations Pages: 45 - 47
Alpha-interferon and fragility at 16q22 Fiorella ShabtaiJerry OrlynIsaac Halbrecht Original Investigations Pages: 48 - 52
Hemoglobin M Iwate is caused by a C→T transition in codon 87 of the human α1-globin gene J. HorstG. AssumE. Kohne Original Investigations Pages: 53 - 55
C-band length variability and reproductive wastage María Teresa Rodriguez-GómezMaría José Martín-SempereJ. A. Abrisqueta Original Investigations Pages: 56 - 61
Association of a DNA polymorphism in the apolipoprotein C-III gene with diverse hyperlipidaemic phenotypes Howard E. HendersonShelley V. LandonG. Michael B. Berger Original Investigations Pages: 62 - 65
Sequences which flank an 11p deletion observed in an hepatocellular carcinoma map to 11p13 J. H. FisherC. H. ScogginC. E. Rogler Original Investigations Pages: 66 - 69
Nineteen of 26 cellular oncogenes precisely localized in the human genome map to one of the 83 bands involved in primary cancer-specific rearrangements S. HeimF. Mitelman Short Communications Pages: 70 - 72
An apparent discrepancy between chain length and electrophoretic mobility of restriction fragments: a case of human mitochondrial DNA Satoshi HoraiTadashi InoueEi Matsunaga Short Communications Pages: 73 - 74
Synergistic effect of aphidicolin and ethanol on the induction of common fragile sites A. KuwanoT. Kajii Short Communications Pages: 75 - 78
DNA-polymorphism of type I collagen gene detected with Bgl II in the genetically isolated finnish population Hannele AhtiAarno PalotieFrancesco Ramirez Short Communications Pages: 79 - 80
Partial androgen receptor deficiency and mixed gonadal dysgenesis in Drash syndrome Catherine TurleauPatrick NiaudetJean de Grouchy Clinical Case Reports Pages: 81 - 83
Familial paracentric inversions inv(2)(q31q35) and inv(8)(q22.3q24.13) ascertained through reproductive abnormalities C. C. LinP. BowenJ. J. Hoo Clinical Case Reports Pages: 84 - 87
A monozygotic twin pair with Rett syndrome G. TariverdianGisela KantnerF. Vogel Clinical Case Reports Pages: 88 - 90
The patient with combined deficiency of neuraminidase and 21-hydroxylase F. HaradaY. NishimuraT. Sasazuki Clinical Case Reports Pages: 91 - 92
Prenatal diagnosis of a 46,XX,inv(12)pat/47,XX,i(Xq),inv(12)pat Maria VarelaNancy WangMabel Cerrillo Clinical Case Reports Pages: 93 - 94
Monosomy 21: a new case confirmed by in situ hybridization M. C. PellissierN. PhilipJ. F. Mattei Clinical Case Reports Pages: 95 - 96
Down syndrome in two siblings with 47,XY,+21 and 46,XY/46,XY,-21,+t(21q;21q) Vazken M. Der KaloustianRola MasriFarid P. Khouri Clinical Case Reports Pages: 97 - 97
Tentative assignment of hypomelanosis of Ito to 9q33→qter Rudolf Happle Letter to the Editors Pages: 98 - 99
