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Nature Genetics|March 1, 2003
Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex diseaseDavid Botstein, Neil RischNature Genetics|March 4, 2003
Mutations in SOX2 cause anophthalmiaJudy Fantes, Nicola K Ragge, Sally-Ann Lynch, et al.Nature Genetics|February 19, 2003
Disruption of Cnp1 uncouples oligodendroglial functions in axonal support and myelinationCorinna Lappe-Siefke, Sandra Goebbels, Michel Gravel, et al.Nature Genetics|April 6, 2004
Duplication-degeneration as a mechanism of gene fission and the origin of new genes in Drosophila speciesWen Wang, Haijing Yu, Manyuan LongNature Genetics|June 11, 2003
14-3-3epsilon is important for neuronal migration by binding to NUDEL: a molecular explanation for Miller-Dieker syndromeKazuhito Toyo-oka, Aki Shionoya, Michael J Gambello, et al.Nature Genetics|June 11, 2003
Cadmium is a mutagen that acts by inhibiting mismatch repairYong Hwan Jin, Alan B Clark, Robbert J C Slebos, et al.Nature Genetics|July 15, 2003
Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the alpha-thalassemia myelodysplasia syndrome (ATMDS)Richard J Gibbons, Andrea Pellagatti, David Garrick, et al.Nature Genetics|July 15, 2003
Mutations in the genes encoding 11beta-hydroxysteroid dehydrogenase type 1 and hexose-6-phosphate dehydrogenase interact to cause cortisone reductase deficiencyNicole Draper, Elizabeth A Walker, Iwona J Bujalska, et al.Nature Genetics|April 1, 1992
Absence of linkage between the angiotensin converting enzyme locus and human essential hypertensionX Jeunemaitre, R P Lifton, S C Hunt, et al.Pageof 744