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Brady KP, Dushkin H, Fornzler D, Koike T, Magner F, Her H, Gullans S, Segre GV, Green RM, and Beier DR (1999). A novel putative transporter maps to the osteosclerosis (oc) mutation and is not expressed in the oc mutant mouse. Genomics 56: 254-261.
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Mao NC, Steingrimsson E, DuHadaway J, Wasserman W, Ruiz JC, Copeland NG, Jenkins NA, and Prendergast GC (1999). The murine Bin1 gene functions early in myogenesis and defines a new region of synteny between mouse chromosome 18 and human chromosome 2. Genomics 56: 51-58.
Matesic LE, De Maio A, and Reeves RH (1999). Mapping lipopolysaccharide response loci in mice using recombinant inbred and congenic strains. Genomics 62: 34-41.
Nakashima H, Grahovac MJ, Mazzarella R, Fujiwara H, Kitchen JR, Threat TA, and Ko MSH (1999). Two novel mouse genes-Nubp2, mapped to the t-complex on chromosome 17, and Nubp1, mapped to chromosome 16 - Establish a new gene family of nucleotide-binding proteins in eukaryotes. Genomics 60: 152-160.
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Shimizu K, Nagamachi Y, Tani M, Kimura K, Shiroishi T, Wakana S, and Yokota J (2000). Molecular cloning of a novel NF2/ERM/4.1 superfamily gene, Ehm2, that is expressed in high-metastatic K1735 murine melanoma cells. Genomics 65: 113-120.
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Hopitzan A, Himmelbauer H, Spevak W, and Castanon MJ (2000). The mouse Psma1 gene coding for the alpha-type C2 proteasome subunit: Structural and functional analysis. mapping, and colocalization with Pde3b on mouse chromosome 7. Genomics 66: 313-323.
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Johnson KR, and Zheng QY (2002). Ahl2, a second locus affecting age-related hearing loss in mice. Genomics 80: 461-464.
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