Galactose-1-phosphate uridyl transferase in density-fractionated erythrocytes Richard I. KelleyDaniel M. FeinbergStanton Segal Original Investigations Pages: 99 - 103
Molecular defects of type III procollagen in Ehlers-Danlos syndrome type IV Andrea Superti-FurgaBeat SteinmannPeter H. Byers Original Investigations Pages: 104 - 108
Two type II keratin genes are localized on human chromosome 12 N. C. PopescuP. E. BowdenJ. A. DiPaolo Original Investigations Pages: 109 - 112
Radioresistant DNA synthesis and human genetic disease Babara R. YoungRobert B. Painter Original Investigations Pages: 113 - 117
Genetic studies of human apolipoproteins B. SepehrniaM. I. KambohR. E. Ferrell Original Investigations Pages: 118 - 122
The aniridia-Wilms' tumour association: molecular and genetic analysis of chromosome deletions on the short arm of chromosome 11 John K. CowellRoy B. WadeyJon Pritchard Original Investigations Pages: 123 - 126
Cytogenetic studies on three pheochromocytomas derived from patients with von Hippel-Lindau syndrome Marion Kiechle-SchwarzHartmut P. H. NeumannWerner Schempp Original Investigations Pages: 127 - 130
A linkage group with FRA16B (the fragile site at 16q22.1) J. C. MulleyV. J. HylandG. R. Sutherland Original Investigations Pages: 131 - 133
Newborn screening by DNA analysis of dried blood spots Edward M. RubinKeith A. AndrewsYuet Wai Kan Original Investigations Pages: 134 - 136
Kinetochore development in two dicentric chromosomes in man Annelise Wandall Original Investigations Pages: 137 - 141
Family and population studies on the human pepsinogen A multigene family J. P. BebelmanM. P. J. EversR. R. Frants Original Investigations Pages: 142 - 146
Nucleolar structures in chromosome and SC preparations from human oocytes at first meiotic prophase M. GarcíaA. DietrichJ. Egozcue Original Investigations Pages: 147 - 153
Centromeric alpha satellite DNA amplification and translocation in an unusually large chromosome 14p+ variant S. DaleE. EarleK. H. Choo Original Investigations Pages: 154 - 158
Determining informativity of marker typing for genetic counseling in a pedigree Lodewijk SandkuylJurg Ott Original Investigations Pages: 159 - 162
Myotonia congenita (Thomsen's disease) excluded from the region of the myotonic dystrophy locus on chromosome 19 Manuela KochHelen HarleyP. S. Harper Original Investigations Pages: 163 - 166
Brachytelephalangic chondrodysplasia punctata: a possible X-linked recessive form P. Maroteaux Original Investigations Pages: 167 - 170
Characterization of a panel of somatic cell hybrids for subregional mapping along 11p and within band 11p13 P. CouillinM. AzoulayC. Junien Original Investigations Pages: 171 - 178
The levels of ζ, γ, and δ chains in patients with Hb H disease Ferdane KutlarJose M. Gonzalez-RedondoTitus H. J. Huisman Original Investigations Pages: 179 - 186
Amplification of satellite III DNA in an unusually large chromosome 14p+ variant E. EarleS. DaleK. H. Choo Original Investigations Pages: 187 - 190
Family study of common fragile sites Yoshitsugu SugioYoshikazu Kuroki Short Communications Pages: 191 - 193
Polyclonal hyper-immunoglobulin G1(A1) syndrome R. W. HendriksL. A. SandkuylR. K. B. Schuurman Short Communications Pages: 194 - 196
Demonstration of spontaneous XX/XY chimerism by DNA fingerprinting C. M. FarberM. GeorgesG. Vassart Short Communications Pages: 197 - 198
Partial trisomy of distal 8q derived from mother with mosaic 8q23.3→24.13 deletion, and relatively mild expression of trichorhinophalangeal syndrome I Kenji NaritomiKiyotake Hirayama Clinical Case Report Pages: 199 - 201
Use of linkage disequilibrium data in prenatal diagnosis of cystic fibrosis D. J. H. BrockSusan Holloway Letter to the Editors Pages: 202 - 202