Replication asynchrony between homologs 15q11.2: Cytogenetic evidence for genomic imprinting Yoshinori IzumikawaKenji NaritomiKiyotake Hirayama Original Investigations Pages: 1 - 5
The size of small polydisperse circular DNA (spcDNA) in angiofibroma-derived cell cultures from patients with tuberous sclerosis (TSC) differs from that in fibroblasts K. MotejlekG. AssumA. K. Kleinschmidt Original Investigations Pages: 6 - 10
Polymorphic DNA haplotypes at the phenylalanine hydroxylase locus and their relation to phenotype in Swedish phenylketonuria families Elisabeth SvenssonUlrika von DöbelnLars Hagenfeldt Original Investigations Pages: 11 - 17
Regional assignment of the human uroporphyrinogen III synthase (UROS) gene to chromosome 10q25.2→q26.3 Kenneth H. AstrinCecilia A. WarnerRobert J. Desnick Original Investigations Pages: 18 - 22
X-linked Charcot-Marie-Tooth disease M. L. MostacciuoloE. MüllerG. A. Danieli Original Investigations Pages: 23 - 27
A novel missense mutation in exon 8 of the ornithine transcarbamylase gene in two unrelated male patients with mild ornithine transcarbamylase deficiency Akira HataToshinobu MatsuuraIchiro Matsuda Original Investigations Pages: 28 - 32
Osteogenesis imperfecta due to recurrent point mutations at CpG dinucleotides in the COL1A1 gene of type I collagen Charles J. PruchnoDaniel H. CohnPeter H. Byers Original Investigations Pages: 33 - 40
Genetic heterogeneity of propionic acidemia: Analysis of 15 Japanese patients Toshihiro OhuraShigeaki MiyabayashiKeiya Tada Original Investigations Pages: 41 - 44
Frequent occurrence of translocations of the short arm of chromosome 15 to other D-group chromosomes Dominique F. C. M. SmeetsGerard F. M. MerkxAnton H. M. Hopman Original Investigations Pages: 45 - 48
Polymorphisms in the human X-linked pyruvate dehydrogenase E1α gene Hans-Henrik M. DahlWendy M. HutchisonLise Lotte Hansen Original Investigations Pages: 49 - 53
A 48,XXY,+21 Down syndrome patient with additional paternal X and maternal 21 Isabel Lorda-SanchezMichael B. PetersenAlbert Schinzel Original Investigations Pages: 54 - 56
Genetic epidemiology of Down's syndrome in Shetland D. F. RobertsM. J. RobertsA. W. Johnston Original Investigations Pages: 57 - 60
Frequency of the F508 deletion in cystic fibrosis patients from the European part of the USSR V. S. BaranovT. E. IvaschenkoN. Y. Shwed Original Investigations Pages: 61 - 64
The physical map of chromosome arm 19q: some new assignments, confirmations and re-assessments J. D. BrookS. J. L. KnightD. J. Shaw Original Investigations Pages: 65 - 72
Localisation of the myotonic dystrophy locus to 19q13.2–19q13.3 and its relationship to twelve polymorphic loci on 19q Helen G. HarleyKate V. WalshDuncan J. Shaw Original Investigations Pages: 73 - 80
Chromosome abnormalities found among 34910 newborn children: results from a 13-year incidence study in Århus, Denmark Johannes NielsenMogens Wohlert Short Communications Pages: 81 - 83
Assignment by in situ hybridization of a fibroblast growth factor receptor gene to human chromosome band 10q26 Marie-Geneviève MatteiAgnès MoreauRichard Breathnach Short Communications Pages: 84 - 86
Population frequency of the arylsulphatase A pseudo-deficiency allele Paul V. NelsonWilliam F. CareyC. Phillip Morris Short Communications Pages: 87 - 88
Genetic polymorphism of inter-alpha-trypsin-inhibitor (ITI): Formal genetic and linkage analyses C. LuckenbachJ. KömpfH. Ritter Short Communications Pages: 89 - 90
Linkage analysis of neurofibromatosis type 1 Maurizio ClementiAlessandra MurgiaFranco Zacchello Short Communications Pages: 91 - 94
Uridine enhances expression of the fragile X chromosome in human lymphocytes Marketta KähkönenRitva HaatajaJaakko Leisti Short Communications Pages: 95 - 96
Aldosterone deficiency II (CMO II deficiency) is not the result of a mutation of an MspI restriction site within the CYP11B gene Antonia MayerovàBarbara ZiegerGerhard Wolff Short Communications Pages: 97 - 98
Carrier detection in haemophilia A by direct analysis of factor VIII gene lesions David S. MillarPeter J. GreenDavid N. Cooper OriginalPaper Pages: 99 - 100
HindIII/Eco RI RFLP of the human immunoglobulin IGHE gene detected with a Cɛ probe in the French and Tunisian populations F. BernardF. DucretM. -P. Lefranc OriginalPaper Pages: 101 - 101
The frequencies of Hbs S and C in Georgia and South Carolina T. H. J. HuismanH. F. HarrisC. Green Letters to the Editors Pages: 102 - 105
Is Shwachman syndrome (McKusick 26040) a chromosome breakage syndrome? Célia P. KoiffmannClaudette H. GonzalezAnita Wajntal Letters to the Editors Pages: 106 - 107
