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Nature Genetics|January 4, 2001
A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophyK Zhang, M Kniazeva, M Han, et al.Nature Genetics|March 10, 2001
Selection for transgene homozygosity in embryonic stem cells results in extensive loss of heterozygosityL Lefebvre, N Dionne, J Karaskova, et al.Nature Genetics|March 10, 2001
Dominant-negative mutations of CEBPA, encoding CCAAT/enhancer binding protein-alpha (C/EBPalpha), in acute myeloid leukemiaT Pabst, B U Mueller, P Zhang, et al.Nature Genetics|March 10, 2001
Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type IJ L Dawkins, D J Hulme, S B Brahmbhatt, et al.Nature Genetics|March 10, 2001
Maternal methylation imprints on human chromosome 15 are established during or after fertilizationO El-Maarri, K Buiting, E G Peery, et al.Nature Genetics|March 30, 2001
Single-nucleotide polymorphisms in the public domain: how useful are they?G Marth, R Yeh, M Minton, et al.Nature Genetics|March 30, 2001
Genetic linkage of childhood atopic dermatitis to psoriasis susceptibility lociW O Cookson, B Ubhi, R Lawrence, et al.Nature Genetics|March 30, 2001
Hepatocyte nuclear factor-1alpha is an essential regulator of bile acid and plasma cholesterol metabolismD Q Shih, M Bussen, E Sehayek, et al.Nature Genetics|March 30, 2001
The amnionless gene, essential for mouse gastrulation, encodes a visceral-endoderm-specific protein with an extracellular cysteine-rich domainS Kalantry, S Manning, O Haub, et al.Nature Genetics|March 30, 2001
Dyssegmental dysplasia, Silverman-Handmaker type, is caused by functional null mutations of the perlecan geneE Arikawa-Hirasawa, W R Wilcox, A H Le, et al.Pageof 743