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Nature Genetics|May 1, 1993
Expression pattern of the Kallmann syndrome gene in the olfactory system suggests a role in neuronal targetingE I Rugarli, B Lutz, S C Kuratani, et al.Nature Genetics|May 1, 1993
Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7qS A Jordan, G J Farrar, P Kenna, et al.Nature Genetics|May 1, 1993
IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndromeR Ohlsson, A Nyström, S Pfeifer-Ohlsson, et al.Nature Genetics|January 1, 1993
A recombination-based assay demonstrates that the fragile X sequence is transcribed widely during developmentA J Hanzlik, M M Osemlak-Hanzlik, M A Hauser, et al.Nature Genetics|January 1, 1993
Neurofibromatosis type 1 gene mutations in neuroblastomaI The, A E Murthy, G E Hannigan, et al.Nature Genetics|March 1, 1996
The quaking gene product necessary in embryogenesis and myelination combines features of RNA binding and signal transduction proteinsT A Ebersole, Q Chen, M J Justice, et al.Nature Genetics|March 1, 1996
Hepatocytes corrected by gene therapy are selected in vivo in a murine model of hereditary tyrosinaemia type IK Overturf, M Al-Dhalimy, R Tanguay, et al.Nature Genetics|March 1, 1996
A recombination hotspot responsible for two inherited peripheral neuropathies is located near a mariner transposon-like elementL T Reiter, T Murakami, T Koeuth, et al.Nature Genetics|March 1, 1996
BRCA1 is secreted and exhibits properties of a graninR A Jensen, M E Thompson, T L Jetton, et al.Nature Genetics|March 1, 1996
The complete BRCA2 gene and mutations in chromosome 13q-linked kindredsS V Tavtigian, J Simard, J Rommens, et al.Pageof 745