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2002 | 1 |
2003 | 1 |
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PubMed for id: 20127399
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Penetrance of craniofacial anomalies in mouse models of Smith-Magenis syndrome is modified by genomic sequence surrounding Rai1: not all null alleles are alike.
Am J Hum Genet. 2007 Mar;80(3):518-25. doi: 10.1086/512043. Epub 2007 Jan 18.
Am J Hum Genet. 2007.
PMID: 17273973
Free PMC article.
Integrated analysis of protein composition, tissue diversity, and gene regulation in mouse mitochondria.
Mootha VK, Bunkenborg J, Olsen JV, Hjerrild M, Wisniewski JR, Stahl E, Bolouri MS, Ray HN, Sihag S, Kamal M, Patterson N, Lander ES, Mann M.
Mootha VK, et al.
Cell. 2003 Nov 26;115(5):629-40. doi: 10.1016/s0092-8674(03)00926-7.
Cell. 2003.
PMID: 14651853
Free article.
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Mouse cytosolic and mitochondrial deoxyribonucleotidases: cDNA cloning of the mitochondrial enzyme, gene structures, chromosomal mapping and comparison with the human orthologs.
Rampazzo C, Kost-Alimova M, Ruzzenente B, Dumanski JP, Bianchi V.
Rampazzo C, et al.
Gene. 2002 Jul 10;294(1-2):109-17. doi: 10.1016/s0378-1119(02)00651-0.
Gene. 2002.
PMID: 12234672
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