Below are the most recent publications written about "Genes, Recessive" by people in Profiles.
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Ghani M, Reitz C, Cheng R, Vardarajan BN, Jun G, Sato C, Naj A, Rajbhandary R, Wang LS, Valladares O, Lin CF, Larson EB, Graff-Radford NR, Evans D, De Jager PL, Crane PK, Buxbaum JD, Murrell JR, Raj T, Ertekin-Taner N, Logue M, Baldwin CT, Green RC, Barnes LL, Cantwell LB, Fallin MD, Go RC, Griffith PA, Obisesan TO, Manly JJ, Lunetta KL, Kamboh MI, Lopez OL, Bennett DA, Hendrie H, Hall KS, Goate AM, Byrd GS, Kukull WA, Foroud TM, Haines JL, Farrer LA, Pericak-Vance MA, Lee JH, Schellenberg GD, St George-Hyslop P, Mayeux R, Rogaeva E. Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals. JAMA Neurol. 2015 Nov; 72(11):1313-23.
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Zhang W, Edwards A, Fan W, Deininger P, Zhang K. Alu distribution and mutation types of cancer genes. BMC Genomics. 2011 Mar 23; 12:157.
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Lee WJ, Bak H, Chang SE, Lee MW, Choi JH, Moon KC, Koh JK. Autosomal recessive type 2 pseudoxanthoma elasticum presenting with generalized skin laxity. J Dermatol. 2009 May; 36(5):288-92.
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McColgan P, Sharma P. The genetics of carotid dissection: meta-analysis of a MTHFR/C677T common molecular variant. Cerebrovasc Dis. 2008; 25(6):561-5.
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Cornier AS, Staehling-Hampton K, Delventhal KM, Saga Y, Caubet JF, Sasaki N, Ellard S, Young E, Ramirez N, Carlo SE, Torres J, Emans JB, Turnpenny PD, Pourqui? O. Mutations in the MESP2 gene cause spondylothoracic dysostosis/Jarcho-Levin syndrome. Am J Hum Genet. 2008 Jun; 82(6):1334-41.
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Kitajiri SI, McNamara R, Makishima T, Husnain T, Zafar AU, Kittles RA, Ahmed ZM, Friedman TB, Riazuddin S, Griffith AJ. Identities, frequencies and origins of TMC1 mutations causing DFNB7/B11 deafness in Pakistan. Clin Genet. 2007 Dec; 72(6):546-50.
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Wilder JA, Hammer MF. European ACP1*C allele has recessive deleterious effects on early life viability. Hum Biol. 2004 Dec; 76(6):817-35.
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McCarrey JR, Abbott UK, Benson DR, Riggins RS. Genetics of scoliosis in chickens. J Hered. 1981 Jan-Feb; 72(1):6-10.