TaqI polymorphism in the LDL receptor gene and a TaqI 1.5-kb band associated with familial hypercholesterolemia Kimiko YamakawaTakaaki OkafujiHideo Hamaguchi Original Investigations Pages: 1 - 5
Maple syrup urine disease: a possible biochemical basis for the clinical heterogeneity Yasuhiro IndoIzumi AkaboshiIchiro Matsuda Original Investigations Pages: 6 - 10
A substitution of cytosine for thymine in codon 110 of the human β-globin gene is a novel cause of β-thalassemia phenotypes Yuji NaritomiYasushi NaitoTakashi Imamura Original Investigations Pages: 11 - 15
X-chromosome polysomy in the male Alice KleczkowskaJean-Pierre FrynsHerman Van den Berghe Original Investigations Pages: 16 - 22
XX sex reversal in the American cocker spaniel dog: phenotypic expression and inheritance Vicki N. Meyers-WallenDonald F. Patterson Original Investigations Pages: 23 - 30
Nephrogenic diabetes insipidus: close linkage with markers from the distal long arm of the human X chromosome N. KnoersH. van der HeydenJ. Willems Original Investigations Pages: 31 - 38
Kenny syndrome: description of additional abnormalities and molecular studies I. BergadaA. SchiffrinG. N. Hendy Original Investigations Pages: 39 - 42
Deletion of chromosome region 13q14 is transmissible and does not always predispose to retinoblastoma John K. CowellPaul RutlandMarcelle Jay Original Investigations Pages: 43 - 45
Maternal levels of pregnancy-specific β1 (SP-1) are elevated in pregnancies affected by Down's syndrome Iris BartelsAndrea Lindemann Original Investigations Pages: 46 - 48
Tight linkage between myotonic dystrophy and apolipoprotein E genes revealed with allele-specific oligonucleotides Bert SmeetsJozef PoddigheBé Wieringa Original Investigations Pages: 49 - 52
Myopia and intelligence:a pleiotropic relationship? Sanford J. CohnCatherine M. G. CohnArthur R. Jensen Original Investigations Pages: 53 - 58
Mapping of the Emery-Dreifuss gene through reconstruction of crossover points in two Italian pedigrees Giovanni RomeoLaura RoncuzziMariano Rocchi Original Investigations Pages: 59 - 62
HLA class I and H ferritin gene polymorphisms in normal subjects and patients with haemochromatosis S. J. CraggC. DarkeM. Worwood Original Investigations Pages: 63 - 68
Hemoglobin F production in heterocellular hereditary persistence of fetal hemoglobin and its linkage to the β globin gene complex J. A. DonaldA. LammiR. J. Trent Original Investigations Pages: 69 - 74
Use of linkage disequilibrium data in prenatal diagnosis of cystic fibrosis Lisa StrainAnn CurtisDavid J. H. Brock Original Investigations Pages: 75 - 77
Allelic association of the cystic fibrosis locus and two DNA markers, XV2c and KM19, in 55 German families M. KrawczakD. S. KoneckiF. K. Trefz Original Investigations Pages: 78 - 80
The parental origin and mechanism of formation of three dicentric X chromosomes Mary C. PhelanLeonard A. ProutyCharles E. Schwartz Original Investigations Pages: 81 - 84
Xp21 DNA microdeletion in a patient with chronic granulomatous disease, retinitis pigmentosa, and McLeod phenotype G. de Saint-BasileM. C. BohlerS. H. Orkin Original Investigations Pages: 85 - 89
β-Globin gene linked DNA haplotypes and frameworks in three South-East Asian populations J. HundrieserT. SanguansermsriG. Flatz Original Investigations Pages: 90 - 94
Fluorescence in situ hybridization and Y ring chromosome Robert KozmaClaudine FearMatteo Adinolfi Short Communications Pages: 95 - 96
Further evidence for localization of the gene of erythrokeratodermia variabilis J. G. van der SchroeffI. van Leeuwen-CornelisseL. N. Went Short Communications Pages: 97 - 98
Recurrent genomic rearrangements are not at the fragile sites on chromosomes 3 and 5 in human renal cell carcinomas G. KovacsP. Brusa Short Communications Pages: 99 - 101
PI Scologne: a new variant in the alpha-1-antitrypsin system W. WeberS. Weidinger Short Communications Pages: 102 - 102
Miller-Dieker syndrome and monosomy 17p13:a new case A. SelypesA. László Clinical Case Reports Pages: 103 - 104
Chondrodysplasia punctata with X;Y translocation Kazunaga AgematsuKenichi KoikeTaro Akabane Clinical Case Reports Pages: 105 - 107
Heterozygosity and localisation of normal allelic fragments for an alpha1-antitrypsin homologous sequence N. A. KalshekerG. L. Watkins DNA Variants Pages: 108 - 109
BglII RFLPs in the COL1A2 gene in the Finnish population Hannele AhtiAarno PalotieLeena Peltonen Letter to the Editors Pages: 110 - 110