Arginase deficiency manifesting delayed clinical sequelae and induction of a kidney arginase isozyme Wayne W. GrodyRita M. KernStephen D. Cederbaum Original Investigations Pages: 1 - 5
Four separate regions on chromosome 17 show loss of heterozygosity in familial breast carcinomas Annika LindblomLambert SkoogCatharina Larsson Original Investigations Pages: 6 - 12
Rapid detection and prevalence of cholesteryl ester transfer protein deficiency caused by an intron 14 splicing defect in hyperalphalipoproteinemia Akihiro InazuJunji KoizumiRyoyu Takeda Original Investigations Pages: 13 - 16
Mapping of the gene for X-chromosomal split-hand/split-foot anomaly to Xq26–q26.1 Mohammad Faiyaz ul HaqueSiegfried UhlhaasPeter Propping Original Investigations Pages: 17 - 19
Aneuploidy detection in human sperm nuclei using fluorescence in situ hybridization Janet M. HolmesRenee H. Martin Original Investigations Pages: 20 - 24
A denaturing gradient gel electrophoresis assay for sensitive detection of p53 mutations John S. BeckAnne E. KwitekVal C. Sheffield Original Investigations Pages: 25 - 30
Localization of a gamma-glutamyl-transferase-related gene family on chromosome 22 Christine MorrisCéline CourtayJohn Groffen Original Investigations Pages: 31 - 36
Evaluation of routine prenatal ultrasound examination in detecting fetal chromosomal abnormalities in a low risk population Claude StollBéatrice DottMarie-Paule Roth Original Investigations Pages: 37 - 41
High-resolution cytogenetic characterization of telomeric associations in ring chromosome 19 Jeffrey R. SawyerRebecca A. RoweChristopher Cunniff Original Investigations Pages: 42 - 44
Polymorphisms in the apolipoprotein B-100 gene contributes to normal variation in plasma lipids in 464 Danish men born in 1948 Peter Steen HansenLars Ulrik GerdesOle Faergeman Original Investigations Pages: 45 - 50
X-linked myoclonus epilepsy explained as a maternally inherited mitochondrial disorder D. Daniëlle de VriesIlse J. de WijsBernard A. van Oost Original Investigations Pages: 51 - 54
Linkage of Van der Woude syndrome (VWS) to REN and exclusion of the candidate gene TGFB2 from the disease locus in a large pedigree A. SanderH. MoserJ. Raveh Original Investigations Pages: 55 - 62
Two new mutations detected by single-strand conformation polymorphism analysis in cystic fibrosis from Russia Tatanya E. IvaschenkoVladislav S. BaranovMichael Dean Original Investigations Pages: 63 - 65
Cystic fibrosis in Spain: high frequency of mutation G542X in the Mediterranean coastal area Teresa CasalsVirginia NunesXavier Estivill Original Investigations Pages: 66 - 70
Hereditary recombined three-allele variant of the Gc system S. KuboO. KitamuraI. Nakasono Short Communications Pages: 71 - 72
Prevalence of common mutations in the arylsulphatase A gene in metachromatic leukodystrophy patients diagnosed in Britain Maria Luiza BarthAnthony FensomAnn Harris Short Communications Pages: 73 - 77
Two cystic fibrosis patients with the genotype G542X/G551D J. ReissU. EllermeyerH. G. Posselt Clinical Case Report Pages: 78 - 79
DXS539, a polymorphic DNA marker proximal of the fragile-X gene J. C. F. M. DreesenJ. A. J. M. van den HurkB. A. van Oost OriginalPaper Pages: 80 - 82
Sequence variant of the human cathepsin G gene B. LüdeckeW. PollerK. Bartholomé OriginalPaper Pages: 83 - 84
Polymorphic tandem repeat region in interleukin-1α intron 6 Sabine BaillyFrancesco S. di GiovineGordon W. Duff OriginalPaper Pages: 85 - 86
D21S210: A highly polymorphic (GT)n marker closely linked to the β-amyloid protein precursor (APP) gene Andrew C. WarrenMelvin G. McInnisStylianos E. Antonarakis OriginalPaper Pages: 87 - 88
Exclusion of the biglycan (BGN) gene as a candidate gene for the Happle syndrome, employing an intragenic single-strand conformational polymorphism Heiko TraupeUlrich VetterHans-Hilger Ropers Letter to the Editors Pages: 89 - 90
