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Nature Genetics|June 16, 1999
Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome. International Hyper-IgD Study GroupJ P Drenth, L Cuisset, G Grateau, et al.Nature Genetics|June 16, 1999
The gene mutated in bare patches and striated mice encodes a novel 3beta-hydroxysteroid dehydrogenaseX Y Liu, A W Dangel, R I Kelley, et al.Nature Genetics|June 16, 1999
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephalyD E Wallis, E Roessler, U Hehr, et al.Nature Genetics|June 16, 1999
A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophyE M Stone, A J Lotery, F L Munier, et al.Nature Genetics|July 3, 1999
Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasisM K Halushka, J B Fan, K Bentley, et al.Nature Genetics|July 3, 1999
Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosaL S Sullivan, J R Heckenlively, S J Bowne, et al.Nature Genetics|July 3, 1999
The lack of chromosomal protein Hmg1 does not disrupt cell growth but causes lethal hypoglycaemia in newborn miceS Calogero, F Grassi, A Aguzzi, et al.Nature Genetics|July 3, 1999
Mutations in a delta 8-delta 7 sterol isomerase in the tattered mouse and X-linked dominant chondrodysplasia punctata. jderry@immunex.comJ M Derry, E Gormally, G D Means, et al.Nature Genetics|July 3, 1999
Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafnessV Labay, T Raz, D Baron, et al.Nature Genetics|July 3, 1999
Mutations in a new gene encoding a thiamine transporter cause thiamine-responsive megaloblastic anaemia syndromeG A Diaz, M Banikazemi, K Oishi, et al.Pageof 745