C-band polymorphisms of chromosome 9: quantification by Ce-bands Kristine WahediIvar Harry Pawlowitzki Original Investigations Pages: 1 - 5
Steroid sulphatase levels are higher in males than in females of the root vole (Microtus oeconomus) Ulf H. WibergKarl Fredga Original Investigations Pages: 6 - 11
Genesis and systematization of cardiovascular anomalies and analysis of skeletal malformations in murine trisomy 16 and 19 C. BacchusH. SterzH. Winking Original Investigations Pages: 12 - 22
An interstitial duplication of the X chromosome in a male allows physical fine mapping of probes from the Xq13-q22 region F. P. M. CremersR. A. PfeifferH. H. Ropers Original Investigations Pages: 23 - 27
Antioxidant status of Fanconi anemia fibroblasts Johan J. P. GilleHeleen M. WortelboerHans Joenje Original Investigations Pages: 28 - 31
Familial hypercholesterolemia in South African Afrikaners P. A. BrinkL. T. SteynD. R. Van der Westhuyzen Original Investigations Pages: 32 - 35
Lack of association and linkage between HLA and familial polyposis coli Masayuki SasakiKenji SugioTakehiko Sasazuki Original Investigations Pages: 36 - 39
Characterization of chromosomes with hybrid genes for Hb Lepore-Washington, Hb Lepore-Baltimore, Hb P-Nilotic, and Hb Kenya K. D. LanclosJ. PattersonT. H. J. Huisman Original Investigations Pages: 40 - 45
p82H identifies sequences at every human centromere Carmen AleixandreDorothy A. MillerOrlando J. Miller Original Investigations Pages: 46 - 50
De novo complex autosomal translocation involving chromosomes 8, 13 and 15 in a girl with a sporadic retinoblastoma E. CalzolariP. PalazziF. Bernardi Original Investigations Pages: 51 - 54
Genetic hemochromatosis and HLA linkage Lawrie W. PowellJanez FerlugaSue Serjeantson Original Investigations Pages: 55 - 56
The human inactivated X chromosome folds in early metaphase, prometaphase, and prophase Daniel L. Van DykeMaria J. WorshamLester Weiss Original Investigations Pages: 57 - 59
Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26–q27 I. OberléG. CamerinoJ. L. Mandel Original Investigations Pages: 60 - 65
Diagnosis of genetic disease using recombinant DNA. Supplement David N. CooperJörg Schmidtke Original Investigations Pages: 66 - 75
PGI*3(Israel), a new, unstable allele in the phosphoglucose isomerase system B. Bonné-TamirS. S. PapihaB. Ramot Original Investigations Pages: 76 - 79
Congenital thyroxine binding globulin deficiency: incidence and inheritance Malcolm B. JenkinsMichael W. Steffes Original Investigations Pages: 80 - 84
Prevalence of the fragile X syndrome in four birth cohorts of children of school age M. KähkönenT. AlitaloJ. Leisti Short Communications Pages: 85 - 87
A small deletion in the Duchenne/Becker muscular dystrophy locus —a functionally important region? K. A. HartA. P. MonacoM. Bobrow Short Communications Pages: 88 - 91
A fragile X female with Down syndrome T. ArinamiI. KondoT. Hirano Clinical Case Report Pages: 92 - 94
