Toward the complete genomic map and molecular pathology of human chromosome 4 Olaf RießBirgit WinkelmannJörg T. Epplen Review Article Pages: 1 - 18
Acceptability of carrier screening for cystic fibrosis during pregnancy in a German population U. JungU. UrnerC. Coutelle Original Investigation Pages: 19 - 24
Parental origin of germ-line and somatic mutations in the retinoblastoma gene Mitsuo V. KatoKanji IshizakiM. V. Kato Original Investigation Pages: 31 - 38
The polymorphism of the plasma inter-α-trypsin inhibitor (ITI) and its relationship to the heavy chain H1 subunit gene (ITIH1) at 3p211-212 Ulrike VogtRichard SesboüéHartwig Cleve Original Investigation Pages: 39 - 44
Genetic polymorphisms of the CST2 locus coding for cystatin SA Masuro ShintaniKiyoshi MinaguchiToshihiko Semba Original Investigation Pages: 45 - 49
Characterization of mutations on the rare duplicated C4/CYP21 haplotype in steroid 21-hydroxylase deficiency Anna WedellBarbro StenglerHolger Luthman Original Investigation Pages: 50 - 54
Molecular characterization and clinical use of a polymorphic tandem repeat in an intron of the human alanine: Glyoxylate aminotransferase gene Christopher J. DanpureGraeme M. BirdseyJennifer Allsop Original Investigation Pages: 55 - 64
Unexpected inactivation of acceptor consensus splice sequence by a −3 C to T transition in intron 2 of the CFTR gene Thierry BienvenuDominique HubertCherif Beldjord Original Investigation Pages: 65 - 68
Chromosomal mapping of human adenylyl cyclase genes type III, type V and type VI N. HaberD. StengelJ. Hanoune Original Investigation Pages: 69 - 73
Supernumerary chromosomes and spermatogenesis in a human male carrier H. JaafarO. Gabriel-RobezY. Rumpler Short Communication Pages: 74 - 76
Identification of deletions in thebtk gene allows unambiguous assessment of carrier status in families with X-linked agammaglobulinaemia Ruth C. LoveringAngela SweatmanChristine Kinnon Short Communication Pages: 77 - 79
Down's syndrome, Edwards' syndrome, Patau's syndrome —synthesis of glycosaminoglycans Valery KukharenkoSvetlana ShelegAlexander Delvig Short Communication Pages: 80 - 82
A study on duplications of the dystrophin gene: Evidence of a geographical difference in the distribution of breakpoints by intron Federico GalvagniFawzy A. SaadCorrado Angelini Short Communication Pages: 83 - 87
Single base pair germ-line deletion in the p53 gene in a cancer predisposed family Richard HamelinFernande BarichardGilles Thomas Short Communication Pages: 88 - 90
A human cDNA coding for the Leydig insulin-like peptide (Ley I-L) E. BurkhardtI. M. AdhamW. Engel Short Communication Pages: 91 - 94
Submicroscopic deletions of 17p13.3 in type 1 Lissencephaly Anne MantelClaude LeonardPierre Landrieu Short Communication Pages: 95 - 96
A deletion in the 5 ′-region of the neurofibromatosis type 1 (NF1) gene Sven HoffmeyerGünter AssumWinfrid Krone Short Communication Pages: 97 - 100
A novel mosaic Bantu/Benin/Bantu βs haplotype found in several African populations Isabel GonçalvesJoão GonçalvesJoão Lavinha Short Communication Pages: 101 - 103
BamHI restriction fragment length polymorphism (RFLP) at the human GST3 gene locus Ajay KumarB. C. DasJ. K. Sharma Rare Genetic Variant Register Pages: 107 - 108
Dinucleotide repeat polymorphism at 11q23 Milhan TelatarPat ConcannonAshhan Tolun DNA Variants Pages: 109 - 109
