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Nature Genetics|June 1, 1994
Sorsby's fundus dystrophy is genetically linked to chromosome 22q13-qterB H Weber, G Vogt, W Wolz, et al.Nature Genetics|June 1, 1994
Cohen syndrome gene assigned to the long arm of chromosome 8 by linkage analysisE Tahvanainen, R Norio, E Karila, et al.Nature Genetics|June 1, 1994
Large scale bacterial gene discovery by similarity searchK Robison, W Gilbert, G M ChurchNature Genetics|July 1, 1994
Alterations in the PITSLRE protein kinase gene complex on chromosome 1p36 in childhood neuroblastomaJ M Lahti, M Valentine, J Xiang, et al.Nature Genetics|July 1, 1994
Germline mutations in the thyrotropin receptor gene cause non-autoimmune autosomal dominant hyperthyroidismL Duprez, J Parma, J Van Sande, et al.Nature Genetics|July 1, 1994
X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1 geneM Jouet, A Rosenthal, G Armstrong, et al.Nature Genetics|July 1, 1994
MASA syndrome is due to mutations in the neural cell adhesion gene L1CAML Vits, G Van Camp, P Coucke, et al.Nature Genetics|March 13, 2002
FACL4, encoding fatty acid-CoA ligase 4, is mutated in nonspecific X-linked mental retardationIlaria Meloni, Maddalena Muscettola, Martine Raynaud, et al.Nature Genetics|April 10, 2002
Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alström syndromeTom Hearn, Glenn L Renforth, Cosma Spalluto, et al.Nature Genetics|March 26, 2002
Genetic analysis of the mouse brain proteomeJoachim Klose, Christina Nock, Marion Herrmann, et al.Pageof 745