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    Results: 1 to 50 of 140

    1.

    A genome-wide association study identifies a novel major locus for glycemic control in type 1 diabetes, as measured by both HbA1c and glucose.

    Paterson AD, Waggott D, Boright AP, Hosseini SM, Shen E, Sylvestre MP, Wong I, Bharaj B, Cleary PA, Lachin JM; MAGIC, Below JE, Nicolae D, Cox NJ, Canty AJ, Sun L, Bull SB; The Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Research Group.

    Diabetes. 2009 Oct 29. [Epub ahead of print]PMID: 19875614 [PubMed - as supplied by publisher]Related articles

    2.

    Genome-wide association identifies the ABO blood group as a major locus associated with serum levels of soluble E-selectin.

    Paterson AD, Lopes-Virella MF, Waggott D, Boright AP, Hosseini SM, Carter RE, Shen E, Mirea L, Bharaj B, Sun L, Bull SB; Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Research Group.

    Arterioscler Thromb Vasc Biol. 2009 Nov;29(11):1958-67. Epub 2009 Sep 3.PMID: 19729612 [PubMed - in process]Related articles

    3.

    Were genome-wide linkage studies a waste of time? Exploiting candidate regions within genome-wide association studies.

    Yoo YJ, Bull SB, Paterson AD, Waggott D, Sun L; The Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Research Group.

    Genet Epidemiol. 2009 Jul 22. [Epub ahead of print]PMID: 19626703 [PubMed - as supplied by publisher]Related articles

    4.

    Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies.

    Nolte IM, Wallace C, Newhouse SJ, Waggott D, Fu J, Soranzo N, Gwilliam R, Deloukas P, Savelieva I, Zheng D, Dalageorgou C, Farrall M, Samani NJ, Connell J, Brown M, Dominiczak A, Lathrop M, Zeggini E, Wain LV; Wellcome Trust Case Control Consortium; DCCT/EDIC Research Group, Newton-Cheh C, Eijgelsheim M, Rice K, de Bakker PI; QTGEN consortium, Pfeufer A, Sanna S, Arking DE; QTSCD consortium, Asselbergs FW, Spector TD, Carter ND, Jeffery S, Tobin M, Caulfield M, Snieder H, Paterson AD, Munroe PB, Jamshidi Y.

    PLoS One. 2009 Jul 9;4(7):e6138.PMID: 19587794 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    Family history of renal disease severity predicts the mutated gene in ADPKD.

    Barua M, Cil O, Paterson AD, Wang K, He N, Dicks E, Parfrey P, Pei Y.

    J Am Soc Nephrol. 2009 Aug;20(8):1833-8. Epub 2009 May 14.PMID: 19443633 [PubMed - indexed for MEDLINE]Related articles

    6.

    Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes.

    Pezzolesi MG, Poznik GD, Mychaleckyj JC, Paterson AD, Barati MT, Klein JB, Ng DP, Placha G, Canani LH, Bochenski J, Waggott D, Merchant ML, Krolewski B, Mirea L, Wanic K, Katavetin P, Kure M, Wolkow P, Dunn JS, Smiles A, Walker WH, Boright AP, Bull SB; DCCT/EDIC Research Group, Doria A, Rogus JJ, Rich SS, Warram JH, Krolewski AS.

    Diabetes. 2009 Jun;58(6):1403-10. Epub 2009 Feb 27.PMID: 19252134 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

    Family-based genetic association study of insulin-like growth factor I microsatellite markers and premenopausal breast cancer risk.

    Fehringer G, Boyd NF, Knight JA, Paterson AD, Dite GS, Giles GG, Southey MC, Andrulis IL, Hopper JL, Ozcelik H.

    Breast Cancer Res Treat. 2009 Nov;118(2):415-24. Epub 2009 Feb 20.PMID: 19229608 [PubMed - in process]Related articles

    8.

    Type 1 diabetes in the BB rat: a polygenic disease.

    Wallis RH, Wang K, Marandi L, Hsieh E, Ning T, Chao GY, Sarmiento J, Paterson AD, Poussier P.

    Diabetes. 2009 Apr;58(4):1007-17. Epub 2009 Jan 23.PMID: 19168599 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    Evidence for pathogenicity of atypical splice mutations in autosomal dominant polycystic kidney disease.

    Wang K, Zhao X, Chan S, Cil O, He N, Song X, Paterson AD, Pei Y.

    Clin J Am Soc Nephrol. 2009 Feb;4(2):442-9. Epub 2009 Jan 21.PMID: 19158373 [PubMed - indexed for MEDLINE]Related articles

    10.

    Mammographic density: a heritable risk factor for breast cancer.

    Boyd NF, Martin LJ, Rommens JM, Paterson AD, Minkin S, Yaffe MJ, Stone J, Hopper JL.

    Methods Mol Biol. 2009;472:343-60. Review.PMID: 19107441 [PubMed - indexed for MEDLINE]Related articles

    11.

    Addendum. CC2D2A, encoding a coiled-coil and C2 domain protein, causes autosomal-recessive mental retardation with retinitis pigmentosa.

    Noor A, Windpassinger C, Patel M, Stachowiak B, Mikhailov A, Azam M, Irfan M, Paterson AD, Lutufullah M, Doherty D, Vincent JB, Ayub M.

    Am J Hum Genet. 2008 Nov;83(5):656. No abstract available. PMID: 19068953 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    Quebec platelet disorder is linked to the urokinase plasminogen activator gene (PLAU) and increases expression of the linked allele in megakaryocytes.

    Diamandis M, Paterson AD, Rommens JM, Veljkovic DK, Blavignac J, Bulman DE, Waye JS, Derome F, Rivard GE, Hayward CP.

    Blood. 2009 Feb 12;113(7):1543-6. Epub 2008 Nov 6.PMID: 18988861 [PubMed - indexed for MEDLINE]Related articlesFree article

    13.

    Unified criteria for ultrasonographic diagnosis of ADPKD.

    Pei Y, Obaji J, Dupuis A, Paterson AD, Magistroni R, Dicks E, Parfrey P, Cramer B, Coto E, Torra R, San Millan JL, Gibson R, Breuning M, Peters D, Ravine D.

    J Am Soc Nephrol. 2009 Jan;20(1):205-12. Epub 2008 Oct 22.PMID: 18945943 [PubMed - indexed for MEDLINE]Related articles

    14.

    Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes.

    Grant SF, Qu HQ, Bradfield JP, Marchand L, Kim CE, Glessner JT, Grabs R, Taback SP, Frackelton EC, Eckert AW, Annaiah K, Lawson ML, Otieno FG, Santa E, Shaner JL, Smith RM, Skraban R, Imielinski M, Chiavacci RM, Grundmeier RW, Stanley CA, Kirsch SE, Waggott D, Paterson AD, Monos DS; DCCT/EDIC Research Group, Polychronakos C, Hakonarson H.

    Diabetes. 2009 Jan;58(1):290-5. Epub 2008 Oct 7.PMID: 18840781 [PubMed - indexed for MEDLINE]Related articlesFree article

    15.

    Association between IGF1 CA microsatellites and mammographic density, anthropometric measures, and circulating IGF-I levels in premenopausal Caucasian women.

    Fehringer G, Ozcelik H, Knight JA, Paterson AD, Boyd NF.

    Breast Cancer Res Treat. 2009 Jul;116(2):413-23. Epub 2008 Sep 11.PMID: 18785005 [PubMed - indexed for MEDLINE]Related articles

    16.

    Reduced proportions of natural killer T cells are present in the relatives of lupus patients and are associated with autoimmunity.

    Wither J, Cai YC, Lim S, McKenzie T, Roslin N, Claudio JO, Cooper GS, Hudson TJ, Paterson AD, Greenwood CM, Gladman D, Pope J, Pineau CA, Smith CD, Hanly JG, Peschken C, Boire G; CaNIOS Investigators, Fortin PR.

    Arthritis Res Ther. 2008;10(5):R108. Epub 2008 Sep 10.PMID: 18783591 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    Identification of LTBP2 on chromosome 14q as a novel candidate gene for bone mineral density variation and fracture risk association.

    Cheung CL, Sham PC, Chan V, Paterson AD, Luk KD, Kung AW.

    J Clin Endocrinol Metab. 2008 Nov;93(11):4448-55. Epub 2008 Aug 12.PMID: 18697872 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    Genome-wide linkage analyses of quantitative and categorical autism subphenotypes.

    Liu XQ, Paterson AD, Szatmari P; Autism Genome Project Consortium.

    Biol Psychiatry. 2008 Oct 1;64(7):561-70. Epub 2008 Jul 16.PMID: 18632090 [PubMed - indexed for MEDLINE]Related articlesFree article

    19.

    Sex, age and generation effects on genome-wide linkage analysis of gene expression in transformed lymphoblasts.

    Rangrej J, Beyene J, Hu P, Paterson AD.

    BMC Proc. 2007;1 Suppl 1:S92. Epub 2007 Dec 18.PMID: 18466596 [PubMed - in process]Related articlesFree article

    20.

    The multiplicity problem in linkage analysis of gene expression data - the power of differentiating cis- and trans-acting regulators.

    Huang B, Rangrej J, Paterson AD, Sun L.

    BMC Proc. 2007;1 Suppl 1:S142. Epub 2007 Dec 18.PMID: 18466486 [PubMed - in process]Related articlesFree article

    21.

    CC2D2A, encoding a coiled-coil and C2 domain protein, causes autosomal-recessive mental retardation with retinitis pigmentosa.

    Noor A, Windpassinger C, Patel M, Stachowiak B, Mikhailov A, Azam M, Irfan M, Siddiqui ZK, Naeem F, Paterson AD, Lutfullah M, Vincent JB, Ayub M.

    Am J Hum Genet. 2008 Apr;82(4):1011-8.PMID: 18387594 [PubMed - indexed for MEDLINE]Related articlesFree article

    22.

    IL5RA and TNFRSF6B gene variants are associated with sporadic IgA nephropathy.

    Liu XQ, Paterson AD, He N, St George-Hyslop P, Rauta V, Gronhagen-Riska C, Laakso M, Thibaudin L, Berthoux F, Cattran D, Pei Y.

    J Am Soc Nephrol. 2008 May;19(5):1025-33. Epub 2008 Feb 6.PMID: 18256354 [PubMed - indexed for MEDLINE]Related articlesFree article

    23.

    Very high and increasing incidence of type 1 diabetes mellitus in Newfoundland and Labrador, Canada.

    Newhook LA, Grant M, Sloka S, Hoque M, Paterson AD, Hagerty D, Curtis J.

    Pediatr Diabetes. 2008 Jun;9(3 Pt 2):62-8. Epub 2008 Jan 24.PMID: 18221421 [PubMed - indexed for MEDLINE]Related articles

    24.

    Molecular diagnostics in autosomal dominant polycystic kidney disease: utility and limitations.

    Zhao X, Paterson AD, Zahirieh A, He N, Wang K, Pei Y.

    Clin J Am Soc Nephrol. 2008 Jan;3(1):146-52. Epub 2007 Dec 12.PMID: 18077784 [PubMed - indexed for MEDLINE]Related articlesFree article

    25.

    Multiple superoxide dismutase 1/splicing factor serine alanine 15 variants are associated with the development and progression of diabetic nephropathy: the Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Genetics study.

    Al-Kateb H, Boright AP, Mirea L, Xie X, Sutradhar R, Mowjoodi A, Bharaj B, Liu M, Bucksa JM, Arends VL, Steffes MW, Cleary PA, Sun W, Lachin JM, Thorner PS, Ho M, McKnight AJ, Maxwell AP, Savage DA, Kidd KK, Kidd JR, Speed WC, Orchard TJ, Miller RG, Sun L, Bull SB, Paterson AD; Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Research Group.

    Diabetes. 2008 Jan;57(1):218-28. Epub 2007 Oct 3.PMID: 17914031 [PubMed - indexed for MEDLINE]Related articlesFree article

    26.

    Genome-wide linkage scan of a large family with IgA nephropathy localizes a novel susceptibility locus to chromosome 2q36.

    Paterson AD, Liu XQ, Wang K, Magistroni R, Song X, Kappel J, Klassen J, Cattran D, St George-Hyslop P, Pei Y.

    J Am Soc Nephrol. 2007 Aug;18(8):2408-15. Epub 2007 Jul 18.PMID: 17634434 [PubMed - indexed for MEDLINE]Related articlesFree article

    27.

    The novel neuronal ceroid lipofuscinosis gene MFSD8 encodes a putative lysosomal transporter.

    Siintola E, Topcu M, Aula N, Lohi H, Minassian BA, Paterson AD, Liu XQ, Wilson C, Lahtinen U, Anttonen AK, Lehesjoki AE.

    Am J Hum Genet. 2007 Jul;81(1):136-46. Epub 2007 May 14.PMID: 17564970 [PubMed - indexed for MEDLINE]Related articlesFree article

    28.

    Multiple variants in vascular endothelial growth factor (VEGFA) are risk factors for time to severe retinopathy in type 1 diabetes: the DCCT/EDIC genetics study.

    Al-Kateb H, Mirea L, Xie X, Sun L, Liu M, Chen H, Bull SB, Boright AP, Paterson AD; DCCT/EDIC Research Group.

    Diabetes. 2007 Aug;56(8):2161-8. Epub 2007 May 18.PMID: 17513698 [PubMed - indexed for MEDLINE]Related articlesFree article

    29.

    The effect of intensive diabetes treatment on resting heart rate in type 1 diabetes: the Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications study.

    Paterson AD, Rutledge BN, Cleary PA, Lachin JM, Crow RS; Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Research Group.

    Diabetes Care. 2007 Aug;30(8):2107-12. Epub 2007 Apr 27.PMID: 17468351 [PubMed - indexed for MEDLINE]Related articlesFree article

    30.

    A novel susceptibility locus on rat chromosome 8 affects spontaneous but not experimentally induced type 1 diabetes.

    Wallis RH, Wang K, Dabrowski D, Marandi L, Ning T, Hsieh E, Paterson AD, Mordes JP, Blankenhorn EP, Poussier P.

    Diabetes. 2007 Jun;56(6):1731-6. Epub 2007 Mar 27.PMID: 17389329 [PubMed - indexed for MEDLINE]Related articlesFree article

    31.

    Mapping autism risk loci using genetic linkage and chromosomal rearrangements.

    Autism Genome Project Consortium, Szatmari P, Paterson AD, Zwaigenbaum L, Roberts W, Brian J, Liu XQ, Vincent JB, Skaug JL, Thompson AP, Senman L, Feuk L, Qian C, Bryson SE, Jones MB, Marshall CR, Scherer SW, Vieland VJ, Bartlett C, Mangin LV, Goedken R, Segre A, Pericak-Vance MA, Cuccaro ML, Gilbert JR, Wright HH, Abramson RK, Betancur C, Bourgeron T, Gillberg C, Leboyer M, Buxbaum JD, Davis KL, Hollander E, Silverman JM, Hallmayer J, Lotspeich L, Sutcliffe JS, Haines JL, Folstein SE, Piven J, Wassink TH, Sheffield V, Geschwind DH, Bucan M, Brown WT, Cantor RM, Constantino JN, Gilliam TC, Herbert M, Lajonchere C, Ledbetter DH, Lese-Martin C, Miller J, Nelson S, Samango-Sprouse CA, Spence S, State M, Tanzi RE, Coon H, Dawson G, Devlin B, Estes A, Flodman P, Klei L, McMahon WM, Minshew N, Munson J, Korvatska E, Rodier PM, Schellenberg GD, Smith M, Spence MA, Stodgell C, Tepper PG, Wijsman EM, Yu CE, Rogé B, Mantoulan C, Wittemeyer K, Poustka A, Felder B, Klauck SM, Schuster C, Poustka F, Bölte S, Feineis-Matthews S, Herbrecht E, Schmötzer G, Tsiantis J, Papanikolaou K, Maestrini E, Bacchelli E, Blasi F, Carone S, Toma C, Van Engeland H, de Jonge M, Kemner C, Koop F, Langemeijer M, Hijmans C, Staal WG, Baird G, Bolton PF, Rutter ML, Weisblatt E, Green J, Aldred C, Wilkinson JA, Pickles A, Le Couteur A, Berney T, McConachie H, Bailey AJ, Francis K, Honeyman G, Hutchinson A, Parr JR, Wallace S, Monaco AP, Barnby G, Kobayashi K, Lamb JA, Sousa I, Sykes N, Cook EH, Guter SJ, Leventhal BL, Salt J, Lord C, Corsello C, Hus V, Weeks DE, Volkmar F, Tauber M, Fombonne E, Shih A, Meyer KJ.

    Nat Genet. 2007 Mar;39(3):319-28. Epub 2007 Feb 18. Erratum in: Nat Genet. 2007 Oct;39(10):1285. Meyer, Kacie J [added]; Koop, Frederike [corrected to Koop, Frederieke]; Langemeijer, Marjolijn [corrected to Langemeijer, Marjolein]; Hijimans, Channa [corrected to Hijmans, Channa]. PMID: 17322880 [PubMed - indexed for MEDLINE]Related articles

    32.

    CRYBA4, a novel human cataract gene, is also involved in microphthalmia.

    Billingsley G, Santhiya ST, Paterson AD, Ogata K, Wodak S, Hosseini SM, Manisastry SM, Vijayalakshmi P, Gopinath PM, Graw J, Héon E.

    Am J Hum Genet. 2006 Oct;79(4):702-9. Epub 2006 Aug 17.PMID: 16960806 [PubMed - indexed for MEDLINE]Related articlesFree article

    33.

    Stratified false discovery control for large-scale hypothesis testing with application to genome-wide association studies.

    Sun L, Craiu RV, Paterson AD, Bull SB.

    Genet Epidemiol. 2006 Sep;30(6):519-30.PMID: 16800000 [PubMed - indexed for MEDLINE]Related articles

    34.

    The role of self-defined race/ethnicity in population structure control.

    Liu XQ, Paterson AD, John EM, Knight JA.

    Ann Hum Genet. 2006 Jul;70(Pt 4):496-505.PMID: 16759181 [PubMed - indexed for MEDLINE]Related articles

    35.

    Effect of environmental factors and gender on the heritability of bone mineral density and bone size.

    Ng MY, Sham PC, Paterson AD, Chan V, Kung AW.

    Ann Hum Genet. 2006 Jul;70(Pt 4):428-38.PMID: 16759177 [PubMed - indexed for MEDLINE]Related articles

    36.

    LDL composition in E2/2 subjects and LDL distribution by Apo E genotype in type 1 diabetes.

    Murdoch SJ, Boright AP, Paterson AD, Zinman B, Steffes M, Cleary P, Edwards K, Marcovina SS, Purnell JQ, Brunzell JD; DCCT/EDIC Research Group.

    Atherosclerosis. 2007 May;192(1):138-47. Epub 2006 Jun 5.PMID: 16740268 [PubMed - indexed for MEDLINE]Related articlesFree article

    37.

    Genetic linkage and association analysis in type 1 von Willebrand disease: results from the Canadian type 1 VWD study.

    James PD, Paterson AD, Notley C, Cameron C, Hegadorn C, Tinlin S, Brown C, O'Brien L, Leggo J, Lillicrap D; ASSOCIATION OF HEMOPHILIA CLINIC DIRECTORS OF CANADA.

    J Thromb Haemost. 2006 Apr;4(4):783-92.PMID: 16634747 [PubMed - indexed for MEDLINE]Related articles

    38.

    Assessment of linkage and association of 13 genetic loci with bone mineral density.

    Lau HH, Ng MY, Cheung WM, Paterson AD, Sham PC, Luk KD, Chan V, Kung AW.

    J Bone Miner Metab. 2006;24(3):226-34.PMID: 16622736 [PubMed - indexed for MEDLINE]Related articles

    39.

    Dynamic microtubules regulate the local concentration of E-cadherin at cell-cell contacts.

    Stehbens SJ, Paterson AD, Crampton MS, Shewan AM, Ferguson C, Akhmanova A, Parton RG, Yap AS.

    J Cell Sci. 2006 May 1;119(Pt 9):1801-11. Epub 2006 Apr 11.PMID: 16608875 [PubMed - indexed for MEDLINE]Related articlesFree article

    40.

    An inversion inv(4)(p12-p15.3) in autistic siblings implicates the 4p GABA receptor gene cluster.

    Vincent JB, Horike SI, Choufani S, Paterson AD, Roberts W, Szatmari P, Weksberg R, Fernandez B, Scherer SW.

    J Med Genet. 2006 May;43(5):429-34. Epub 2006 Mar 23.PMID: 16556609 [PubMed - indexed for MEDLINE]Related articlesFree article

    41.

    Genetic epidemiology of type 1 diabetes.

    Paterson AD.

    Curr Diab Rep. 2006 Apr;6(2):139-46. Review.PMID: 16542625 [PubMed - indexed for MEDLINE]Related articles

    42.

    A genome scan for parent-of-origin linkage effects in alcoholism.

    Liu XQ, Greenwood CM, Wang KS, Paterson AD.

    BMC Genet. 2005 Dec 30;6 Suppl 1:S160. [Epub ahead of print]PMID: 16451622 [PubMed - as supplied by publisher]Related articlesFree article

    43.

    Evaluating outlier loci and their effect on the identification of pedigree errors.

    Wang KS, Liu M, Paterson AD.

    BMC Genet. 2005 Dec 30;6 Suppl 1:S155. [Epub ahead of print]PMID: 16451616 [PubMed - as supplied by publisher]Related articlesFree article

    44.

    An analysis of identical single-nucleotide polymorphisms genotyped by two different platforms.

    Suarez BK, Taylor C, Bertelsen S, Bierut LJ, Dunn G, Jin CH, Kauwe JS, Paterson AD, Hinrichs AL.

    BMC Genet. 2005 Dec 30;6 Suppl 1:S152. [Epub ahead of print]PMID: 16451613 [PubMed - as supplied by publisher]Related articlesFree article

    45.

    Genetic Analysis Workshop 14: microsatellite and single-nucleotide polymorphism marker loci for genome-wide scans.

    Bailey-Wilson JE, Almasy L, de Andrade M, Bailey J, Bickeböller H, Cordell HJ, Daw EW, Goldin L, Goode EL, Gray-McGuire C, Hening W, Jarvik G, Maher BS, Mendell N, Paterson AD, Rice J, Satten G, Suarez B, Vieland V, Wilcox M, Zhang H, Ziegler A, Maccluer JW.

    BMC Genet. 2005 Dec 30;6 Suppl 1:S1. [Epub ahead of print]PMID: 16451554 [PubMed - as supplied by publisher]Related articlesFree article

    46.

    Mammographic breast density as an intermediate phenotype for breast cancer.

    Boyd NF, Rommens JM, Vogt K, Lee V, Hopper JL, Yaffe MJ, Paterson AD.

    Lancet Oncol. 2005 Oct;6(10):798-808. Review. Erratum in: Lancet Oncol. 2005 Nov;6(11):826. PMID: 16198986 [PubMed - indexed for MEDLINE]Related articles

    48.

    Sex-specific effect of insulin-dependent diabetes 4 on regulation of diabetes pathogenesis in the nonobese diabetic mouse.

    Ivakine EA, Fox CJ, Paterson AD, Mortin-Toth SM, Canty A, Walton DS, Aleksa K, Ito S, Danska JS.

    J Immunol. 2005 Jun 1;174(11):7129-40.PMID: 15905556 [PubMed - indexed for MEDLINE]Related articlesFree article

    49.

    ANKH variants associated with ankylosing spondylitis: gender differences.

    Tsui HW, Inman RD, Paterson AD, Reveille JD, Tsui FW.

    Arthritis Res Ther. 2005;7(3):R513-25. Epub 2005 Feb 25.PMID: 15899038 [PubMed - indexed for MEDLINE]Related articlesFree article

    50.

    Search for genetic variants associated with cutaneous malignant melanoma in the Ashkenazi Jewish population.

    Loo JC, Paterson AD, Hao A, Shennan M, Peretz H, Sidi Y, Hogg D, Yakobson E.

    J Med Genet. 2005 May;42(5):e30. No abstract available. PMID: 15863662 [PubMed - indexed for MEDLINE]Related articlesFree article

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