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Nature Genetics|April 1, 1993
A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3H Watkins, C MacRae, L Thierfelder, et al.Nature Genetics|April 1, 1993
Cartilage-hair hypoplasia gene assigned to chromosome 9 by linkage analysisT Sulisalo, P Sistonen, J Hästbacka, et al.Nature Genetics|April 2, 2002
Disruption of an SF2/ASF-dependent exonic splicing enhancer in SMN2 causes spinal muscular atrophy in the absence of SMN1Luca Cartegni, Adrian R KrainerNature Genetics|April 2, 2002
Adaptive evolution of a duplicated pancreatic ribonuclease gene in a leaf-eating monkeyJianzhi Zhang, Ya-ping Zhang, Helene F RosenbergNature Genetics|April 23, 2002
Disruption of CREB function in brain leads to neurodegenerationTheo Mantamadiotis, Thomas Lemberger, Susanne C Bleckmann, et al.Nature Genetics|March 13, 2002
Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsyPetter Strømme, Marie E Mangelsdorf, Marie A Shaw, et al.Nature Genetics|March 16, 2002
Haploinsufficiency of NSD1 causes Sotos syndromeNaohiro Kurotaki, Kiyoshi Imaizumi, Naoki Harada, et al.Nature Genetics|November 1, 1994
Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11L P Ranum, L J Schut, J K Lundgren, et al.Nature Genetics|November 1, 1994
A possible vulnerability locus for bipolar affective disorder on chromosome 21q22.3R E Straub, T Lehner, Y Luo, et al.Nature Genetics|November 1, 1994
Autosomal dominant hypocalcaemia caused by a Ca(2+)-sensing receptor gene mutationM R Pollak, E M Brown, H L Estep, et al.Pageof 743