Why is the cystic fibrosis gene so frequent? Giovanni RomeoMarcella DevotoLuis Juan Vicente Galietta Review Article Pages: 1 - 5
Localization of the active type I DNA topoisomerase gene on human chromosome 20q11.2-13.1, and two pseudogenes on chromosomes 1q23-24 and 22q11.2-13.1 N. KunzeG. C. YangR. Knippers Original Investigations Pages: 6 - 10
Linkage of PGK1 to X-linked severe combined immunodeficiency (IMD4) allows predictive testing in families with no surviving male Judith GoodshipRoland LevinskySue Malcolm Original Investigations Pages: 11 - 14
G2 chromosomal radiosensitivity in families with ataxia-telangiectasia Yosef ShilohRam ParshadGary M. Jones Original Investigations Pages: 15 - 18
Close linkage of probe p212 (DXS178) to X-linked agammaglobulinemia S. GuioliB. ArveilerG. Camerino Original Investigations Pages: 19 - 21
Physical fine-mapping of a deletion spanning the Norrie gene P. J. DiergaardeB. WieringaH. -H. Ropers Original Investigations Pages: 22 - 26
The volumes and morphology of human chromosomes in mitotic reconstructions J. S. Heslop-HarrisonA. R. LeitchM. D. Bennett Original Investigations Pages: 27 - 34
Increased detectability of somatic changes in the DNA from human tumours after probing with “synthetic” and “genome-derived” hypervariable multilocus probes P. J. L. LagodaG. SeitzO. -G. Issinger Original Investigations Pages: 35 - 40
Molecular basis of β-thalassemia in Thailand: analysis of β-thalassemia mutations using the polymerase chain reaction Supan FucharoenGoonnapa FucharoenYasuyuki Fukumaki Original Investigations Pages: 41 - 46
The spectrum of β-thalassemia mutations in northern and northeastern Thailand Marion LaigT. SanguansermsriG. Flatz Original Investigations Pages: 47 - 50
Cytogenetic and molecular analysis of an unbalanced translocation (X;7) (q28;p15) in a dysmorphic girl A. CaiuloB. BardoniP. Maraschio Original Investigations Pages: 51 - 54
Molecular characterisation of three alpha-1-antitrypsin deficiency variants: proteinase inhibitor (Pi) nullcardiff (Asp256→Val); Pi Mmalton (Phe51→ deletion) and Pi I (Arg39→Cys) Alexander GrahamNoor A. KalshekerAlexander F. Markham Original Investigations Pages: 55 - 58
The gene encoding the human preproacrosin (ACR) maps to the q13-qter region on chromosome 22 I. M. AdhamK. -H. GrzeschikW. Engel Original Investigations Pages: 59 - 62
Isochromosome not translocation in trisomy 21q21q M. GrassoM. L. Giovannucci UzielliF. Dagna Bricarelli Original Investigations Pages: 63 - 65
Haplotype and multipoint linkage analysis in Finnish choroideremia families Eeva-Marja SankilaThomas LehnerAlbert de la Chapelle Original Investigations Pages: 66 - 70
Cell type-dependent difference in the distribution and frequency of aphidicolin-induced fragile sites: T and B lymphocytes and bone marrow cells Ichiro MuranoAkira KuwanoTadashi Kajii Original Investigations Pages: 71 - 74
DNA Fingerprinting with the oligonucleotide probe (CAC)5/(GTG)5: somatic stability and germline mutations P. NürnbergL. RoewerJ. T. Epplen Original Investigations Pages: 75 - 78
Gene assignment of Zellweger syndrome to 7q11.23: report of the second case associated with a pericentric inversion of chromosome 7 Kenji NaritomiYoshinori IzumikawaKiyotake Hirayama Short Communications Pages: 79 - 80
Rate of chromosomal aberrations in prenatally detected hydrops fetalis and hygroma colli G. SchwanitzK. ZerresM. Hansmann Short Communications Pages: 81 - 82
Prenatal enzymatic diagnosis of Krabbe disease (globoid-cell leukodystrophy) using chorionic villi K. HarzerI. Schuster Short Communications Pages: 83 - 85
A search for restriction fragment length polymorphism on the human Y chromosome Sibylle JakubiczkaJoachim ArnemannJörg Schmidtke Short Communications Pages: 86 - 88
Use of transgenic mice for the characterization of human alpha 1-acid glycoprotein (orosomucoid) variants L. TomeiC. B. EapL. Dente Short Communications Pages: 89 - 91
Human interferon gamma receptor 1 (IFNGR1) gene maps to chromosome region 6q23–6q24 Maryvonne Le ConiatCatherine Alcaide-LoridanRoland Berger Short Communications Pages: 92 - 94
Phenylketonuria: detection of a frequent haplotype 4 allele mutation Bernd DworniczakChrista Aulehla-ScholzJürgen Horst Short Communications Pages: 95 - 96
Unusual chromosome 20 anomaly arising “de novo” to give dic(20)qs Dolores PimentelPilar AlonsoJ. A. Abrisqueta Clinical Case Report Pages: 97 - 98
No lack of complementation for unscheduled DNA synthesis between xeroderma pigmentosum complementation groups D and H Jay H. Robbins Letters to the Editors Pages: 99 - 100
