Intrachromosomal insertions: a case report and a review K. MadanF. H. Menko Review Article Pages: 1 - 9
Confirmation of the human cathepsin B gene (CTSB) assignment to chromosome 8 Dunne FongMarion Man-Ying ChanDavid C. Ward Original Investigations Pages: 10 - 12
Chromosome-band-specific painting: chromosome in situ suppression hybridization using PCR products from a microdissected chromosome band as a probe pool Han-Xiang DengKoh-ichiro YoshiuraNorio Niikawa Original Investigations Pages: 13 - 17
Dual fluorescent in situ hybridisation for simultaneous detection of X and Y chromosome-specific probes for the sexing of human preimplantation embryonic nuclei Darren K. GriffinLeeanda J. WiltonJoy D. A. Delhanty Original Investigations Pages: 18 - 22
Molecular cytogenetic analysis of XX males using Y-specific DNA sequences, including SRY B. Van der AuweraN. Van RoyF. Speleman Original Investigations Pages: 23 - 28
Point mutations in the upstream region of the α-galactosidase A gene exon 6 in an atypical variant of Fabry disease Satoshi IshiiHitoshi SakurabaYoshiyuki Suzuki Original Investigations Pages: 29 - 32
Anonymous markers located on chromosome 6 in the HLA-A class I region: allelic distribution in genetic haemochromatosis Joëlle BorettoAnne-Marie JouanolleVéronique David Original Investigations Pages: 33 - 36
ααααanti-3.7 type II: a new α-globin gene rearrangement suggesting that the α-globin gene duplication could be caused by intrachromosomal recombination M. De AngiolettiG. LacerraC. Carestia Original Investigations Pages: 37 - 41
Abnormal lymphokine production: a novel feature of the genetic disease Fanconi anemia F. RosselliJ. SanceauE. Moustacchi Original Investigations Pages: 42 - 48
Detection of small RB1 gene deletions in retinoblastoma by multiplex PCR and high-resolution gel electrophoresis Dietmar LohmannBernhard HorsthemkeHeinz Höfler Original Investigations Pages: 49 - 53
Confirmation of linkage of benign familial neonatal convulsions to D20S19 and D20S20 Alain MalafosseMarion LeboyerJacques Mallet Original Investigations Pages: 54 - 58
Allotype distribution of human T cell receptor β and γ chain genes in Caucasians, Asians and Australian Aborigines: Relevance to chronic hepatitis B Purnomo SoeharsoKim M. SummersW. G. E. Cooksley Original Investigations Pages: 59 - 63
Cytogenetic, oncogenetic, and histopathologic characteristics of colorectal carcinomas with 17p abnormalities D. RauS. NeubauerE. Gebhart Original Investigations Pages: 64 - 68
Linkage disequilibrium between phenylketonuria and RFLP haplotype 1 at the phenylalanine hydroxylase locus in Portugal Catherine CaillaudLaura VilarinhoArnold Munnich Original Investigations Pages: 69 - 72
Isolation of anonymous DNA markers for human chromosome 22q11 from a flow-sorted library, and mapping using hybrids from patients with DiGeorge syndrome A. M. SharkeyL. McLarenH. J. Evans Original Investigations Pages: 73 - 78
Assignment of casein kinase 2 alpha sequences to two different human chromosomes Brigitte BoldyreffChristine KlettOlaf-Georg Issinger Original Investigations Pages: 79 - 82
The French Canadian Tay-Sachs disease deletion mutation: identification of probable founders M. De BraekeleerP. HechtmanF. Kaplan Original Investigations Pages: 83 - 87
Screening for nonsense mutations in patients with severe hemophilia A can provide rapid, direct carrier detection Alexander P. ReinerArthur R. Thompson Original Investigations Pages: 88 - 94
Canadian Mennonites and individuals residing in the Friesland region of the Netherlands share the same molecular basis of 17α-hydroxylase deficiency Tsuneo ImaiToshihiko YanaseJohn J. Pratt Original Investigations Pages: 95 - 96
Homozygous acute intermittent porphyria: compound heterozygosity for adjacent base transitions in the same codon of the porphobilinogen deaminase gene D. H. LlewellynS. J. SmythM. F. Smith Original Investigations Pages: 97 - 98
βs Haplotypes in various world populations Cihan ÖnerAleksandar J. DimovskiTitus H. J. Huisman Original Investigations Pages: 99 - 104
Regional chromosomal assignment of the human platelet phosphofructokinase gene to 10p15 Norma MorrisonCraig SimpsonJ. Michael Connor Short Communications Pages: 105 - 106
The gene for the human IgA Fc receptor maps to 19q13.4 E. J. KremerV. KalatzisC. R. Maliszewski Short Communications Pages: 107 - 108
Prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia using the polymerase chain reaction David OwerbachMartin B. DrazninFrank Greenberg Short Communications Pages: 109 - 110
Glucose-6-phosphate dehydrogenase (G6PD) electrophoretic variants and the PvuII polymorphism in Southern African populations Marius J. CoetzeeSharon C. BartleetTrefor Jenkins Short Communications Pages: 111 - 113
Genotype mosaicism in fragile X fetal tissues Doris WöhrleMark C. HirstPeter Steinbach Short Communications Pages: 114 - 116
Sperm chromosome analysis of a man heterozygous for a pericentric inversion of chromosome 20 J. JendernyJ. GebauerA. Rüger Short Communications Pages: 117 - 119
Alport syndrome caused by a 5′ deletion within the COL4A5 gene Alessandra RenieriMarco SeriMario De Marchi Short Communications Pages: 120 - 121
A rare MspI RFLP of the DMD probe p20 (DXS269) S. UhlhaasE. BakkerW. Friedl OriginalPaper Pages: 122 - 122
Highly polymorphic region of the human prothrombin (F2) gene Hiroyuki IwahanaKatsuhiko YoshimotoMitsuo Itakura OriginalPaper Pages: 123 - 124
A comment on the paper: Ovarian dysgenesis in individuals with chromosomal abnormalities, by C. Cunniff, K. Lyons Jones, and K. Benirschke P. H. Jongbloet Letter to the Editors Pages: 125 - 125