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Nature Genetics|May 1, 1993
Origin of the expansion mutation in myotonic dystrophyG Imbert, C Kretz, K Johnson, et al.Nature Genetics|January 1, 1996
Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmiasQ Wang, M E Curran, I Splawski, et al.Nature Genetics|January 1, 1996
Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporterD B Simon, C Nelson-Williams, M J Bia, et al.Nature Genetics|January 1, 1996
Chromosomal mapping of genetic loci associated with non-insulin dependent diabetes in the GK ratD Gauguier, P Froguel, V Parent, et al.Nature Genetics|February 1, 1993
Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesisE Legius, D A Marchuk, F S Collins, et al.Nature Genetics|February 1, 1993
X-chromosome inactivation occurs at different times in different tissues of the post-implantation mouse embryoS S Tan, E A Williams, P P TamNature Genetics|January 1, 1993
Isolation of a partial candidate gene for Menkes disease by positional cloningJ F Mercer, J Livingston, B Hall, et al.Nature Genetics|January 1, 1993
Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndromeH L Hinds, C T Ashley, J S Sutcliffe, et al.Nature Genetics|January 1, 1993
Large deletions and other gross forms of chromosome imbalance compatible with viability and fertility in the mouseB M Cattanach, M D Burtenshaw, C Rasberry, et al.Nature Genetics|January 1, 1993
Evidence for a new tumour suppressor locus (DBM) in human B-cell neoplasia telomeric to the retinoblastoma geneA G Brown, F M Ross, E M Dunne, et al.Pageof 744