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Nature Genetics|May 1, 1997
Many human L1 elements are capable of retrotranspositionD M Sassaman, B A Dombroski, J V Moran, et al.Nature Genetics|May 1, 1997
Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndromeD Liaw, D J Marsh, J Li, et al.Nature Genetics|May 1, 1997
Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomasL Schmidt, F M Duh, F Chen, et al.Nature Genetics|May 1, 1997
Mutations in PMM2, a phosphomannomutase gene on chromosome 16p13, in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome)G Matthijs, E Schollen, E Pardon, et al.Nature Genetics|May 1, 1997
Tissue-specific selection for different mtDNA genotypes in heteroplasmic miceJ P Jenuth, A C Peterson, E A ShoubridgeNature Genetics|May 1, 1997
Global distribution of the CCR5 gene 32-basepair deletionJ J Martinson, N H Chapman, D C Rees, et al.Nature Genetics|January 23, 1999
Options available--from start to finish--for obtaining expression data by microarrayD D BowtellNature Genetics|January 23, 1999
DNA microarrays in drug discovery and developmentC Debouck, P N GoodfellowNature Genetics|January 23, 1999
Gene expression informatics--it's all in your mineD E Bassett, M B Eisen, M S BoguskiNature Genetics|January 23, 1999
Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafnessF E Karet, K E Finberg, R D Nelson, et al.Pageof 745