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Montgomery, G. W., Zhao, Z. Z., Marsh, A. J., Mayne, R., Treloar, S. A., James, M., Martin, N. G., Boomsma, D. I. and Duffy, D. L. (2004) A deletion mutation in GDF9 in sisters with spontaneous DZ twins. Twin Research, 7 6: 548-555. doi:10.1375/1369052042663823 96   41 Cited 44 times in Scopus44 0
Shekar, Sri Niranjan, Duffy, David L., Montgomery, Grant W. and Martin, Nicholas G. (2006) A genome scan for epidermal skin pattern in adolescent twins reveals suggestive linkage on 12p13.31. Journal of Investigative Dermatology, 126 2: 277-282. doi:10.1038/sj.jid.5700067 73   1 Cited 1 times in Scopus1 0
Zhu, G., Evans, D. M., Duffy, D. L., Montgomery, G. W., Medland, S. E., Gillespie, N. A., Ewen, K. R., Jewell, M., Liew, Y. W., Hayward, N. K., Sturm, R. A., Trent, J. M. and Martin, N. G. (2004) A genome scan for eye color in 502 twin families: Most variation is due to a QTL on chromosome 15q. Twin Research, 7 2: 197-210. doi:10.1375/136905204323016186 143   79 Cited 87 times in Scopus87 3
Han, J., Kraft, P., Nan, H., Guo, Q., Chen, C., Qureshi, A., Hankinson, S.E., Hu, F.B., Duffy, D., Zhao, Z.Z., Martin, N. G., Montgomery, G., Hayward, N., Thomas, G., Hoover, R.N., Chanock, S. and Hunter, D.J. (2008) A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. Plos Genetics, 4 5: e1000074. doi:10.1371/journal.pgen.1000074 106   136 Cited 163 times in Scopus163 27
Painter, Jodie N., Willemsen, Gonneke, Nyholt, Dale, Hoekstra, Chantal, Duffy, David L., Henders, Anjali K., Wallace, Leanne, Healey, Sue, Cannon-Albright, Lisa A., Skolnick, Mark, Martin, Nicholas G., Boomsma, Dorret I. and Montgomery, Grant W. (2010) A genome wide linkage scan for dizygotic twinning in 525 families of mothers of dizygotic twins. Human Reproduction, 25 6: 1569-1580. doi:10.1093/humrep/deq084 111   7 Cited 10 times in Scopus10 0
Zhu, Gu, Montgomery, Grant W., James, Michael R., Trent, Jeff M., Hayward, Nicholas K., Martin, Nicholas G. and Duffy, David L. (2007) A genome-wide scan for naevus count: Linkage to CDKN2A and to other chromosome regions. European Journal of Human Genetics, 15 1: 94-102. doi:10.1038/sj.ejhg.5201729 102   45 Cited 47 times in Scopus47 0
Busfield, Frances, Duffy, David L., Kesting, Janine B., Walker, Shelley M., Lovelock, Paul K., Good, David, Tate, Heather, Watego, Denise, Marczak, Maureen, Hayman, Noel and Shaw, Joanne T. E. (2002) A genomewide search for type 2 diabetes-susceptibility genes in indigenous Australians. American Journal of Human Genetics, 70 2: 349-357. doi:10.1086/338626 140   56 Cited 60 times in Scopus60 0
Luciano, Michelle, Lind, Penelope A., Duffy, David L., Castles, Anne, Wright, Margaret J., Montgomery, Grant W., Martin, Nicholas G. and Bates, Timothy C. (2007) A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability. Biological Psychiatry, 62 7: 811-817. doi:10.1016/j.biopsych.2007.03.007 84   53 Cited 53 times in Scopus53 3
Evans, D. M., Zhu, G., Duffy, D. L., Frazer, I. H., Montgomery, G. W. and Martin, N. G. (2004) A major quantitative trait locus for CD4-CD8 ratio is located on chromosome 11. Genes and Immunity, 5 7: 548-552. doi:10.1038/sj.gene.6364126 192   11 Cited 10 times in Scopus10 0
Zhu, G, Duffy, DL, Eldridge, A, Grace, M, Mayne, C, O'Gorman, L, Aitken, JF, Neale, MC, Hayward, NK, Green, AC and Martin, NG (1999) A major quantitative-trait locus for mole density is linked to the familial melanoma gene CDKN2A: a maximum-likelihood combined linkage and association analysis in twins and their sibs. American Journal of Human Genetics, 65 2: 483-492. doi:10.1086/302494 78   146 Cited 159 times in Scopus159 0
Cook, Anthony L., Chen, Wei, Thurber, Amy E., Smit, Darren J., Smith, Aaron G., Bladen, Timothy G., Brown, Darren L., Duffy, David L., Pastorino, Lorenza, Bianchi-Scarra, Giovanna, Leonard, J. Helen, Stow, Jennifer L. and Sturm, Richard A. (2009) Analysis of Cultured Human Melanocytes Based on Polymorphisms within the SLC45A2/MATP, SLC24A5/NCKX5, and OCA2/P Loci. Journal of Investigative Dermatology, 129 2: 392-405. doi:10.1038/jid.2008.211 99   40 Cited 44 times in Scopus44 18
Yokoyama, Satoru, Woods, Susan L., Boyle, Glen M., Aoude, Lauren G., MacGregor, Stuart, Zismann, Victoria, Gartside, Michael, Cust, Anne E., Haq, Rizwan, Harland, Mark, Taylor, John C., Duffy, David L., Holohan, Kelly, Dutton-Regester, Ken, Palmer, Jane M., Bonazzi, Vanessa, Stark, Mitchell S., Symmons, Judith, Law, Matthew H., Schmidt, Christopher, Lanagan, Cathy, O'Connor, Linda, Holland, Elizabeth A., Schmid, Helen, Maskiell, Judith A., Jetann, Jodie, Ferguson, Megan, Jenkins, Mark A., Kefford, Richard F., Giles, Graham G., Armstrong, Bruce K., Aitken, Joanne F., Hopper, John L., Whiteman, David C., Pharoah, Paul D., Easton, Douglas F., Dunning, Alison M., Newton-Bishop, Julia A., Montgomery, Grant W., Martin, Nicholas G., Mann, Graham J., Bishop, D. Timothy, Tsao, Hensin, Trent, Jeffrey M., Fisher, David E., Hayward, Nicholas K. and Brown, Kevin M. (2011) A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma. Nature, 480 7375: 99-103. doi:10.1038/nature10630 159 3 101 Cited 109 times in Scopus109 11
Lose, F., Thompson, P. J., Duffy, D., Stewart, G. A. and Kedda, M. -A. (2005) A novel tissue inhibitor of metalloproteinase-1 (TIMP-1) polymorphism associated with asthma in Australian women. Thorax, 60 8: 623-628. doi:10.1136/thx.2004.026930 32   31 Cited 35 times in Scopus35 0
Shekar, SN, Duffy, DL, Youl, P, Baxter, AJ, Kvaskoff, M, Whiteman, DC, Green, AC, Hughes, MC, Hayward, NK, Coates, M and Martin, NG (2009) A Population-Based Study of Australian Twins with Melanoma Suggests a Strong Genetic Contribution to Liability. Journal of Investigative Dermatology, 129 9: 2211-2219. doi:10.1038/jid.2009.48 79   11 Cited 12 times in Scopus12 0
Duffy, D. L. (2001) Applying statistical approaches in the dissection of genes versus environment for asthma and allergic disease. Current Opinion in Allergy & Clinical Immunology, 1 5: 431-434. 45  
Ferreira, Manuel A. R., Visscher, Peter M., Martin, Nicholas G. and Duffy, David L. (2006) A simple method to localise pleiotropic susceptibility loci using univariate linkage analyses of correlated traits. European Journal of Human Genetics, 14 8: 953-962. doi:10.1038/sj.ejhg.5201646 59   7 Cited 7 times in Scopus7 0
Sturm, Richard A., Duffy, David L., Zhao, Zhen Zhen, Leite, Fabio P.N., Stark, Mitchell S., Hayward, Nicholas K., Martin, Nicholas G. and Montgomery, Grant W. (2008) A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye colour. The American Journal of Human Genetics, 82 2: 424-431. doi:10.1016/j.ajhg.2007.11.005 85   132 Cited 137 times in Scopus137 16
Ferreira, M. A. R., Zhao, Z. Z., Thomsen, S. F., James, M., Evans, D. M., Postmus, P. E., Kyvik, K. O., Backer, V., Boomsma, D. I., Martin, N. G., Montgomery, G. W. and Duffy, D. L. (2009) Association and interaction analyses of eight genes under asthma linkage peaks. Allergy, 64 11: 1623-1628. doi:10.1111/j.1398-9995.2009.02091.x 53   6 Cited 6 times in Scopus6 0
Treloar, Susan A., Zhao, Zhen Zhen, Armitage, Trudi, Duffy, David L., Wicks, Jacqueline, O'Connor, Daniel T., Martin, Nicholas G. and Montgomery, Grant W. (2005) Association between polymorphisms in the progesterone receptor gene and endometriosis. Molecular Human Reproduction, 11 9: 641-647. doi:10.1093/molehr/gah221 101 100 21 Cited 23 times in Scopus23 0
Byrne, EM, McRae, AF, Duffy, DL, Zhao, ZZ, Martin, NG, Wright, MJ, Montgomery, GW and Visscher, PM (2009) Association Study of Common Mitochondrial Variants and Cognitive Ability. BEHAVIOR GENETICS, 39 5: 504-512. doi:10.1007/s10519-009-9276-x 57   2 Cited 2 times in Scopus2 6
Condon, Julianne, Shaw, Joanne E., Luciano, Michelle, Kyvik, Kirsten O., Martin, Nicholas G. and Duffy, David L. (2008) A study of diabetes mellitus within a large sample of Australian twins. Twin Research and Human Genetics, 11 1: 28-40. doi:10.1375/twin.11.1.28 41   13 Cited 14 times in Scopus14 0
Duffy, D. L., Montgomery, G. W., Chen, W., Zhao, Z. Z., Le, L., James, M. R., Hayward, N. K., Martin, N. G. and Sturm, R. A. (2007) A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation. American Journal of Human Genetics, 80 2: 241-252. doi:10.1086/510885 137   99 Cited 114 times in Scopus114 6
James, Michael R., Roth, Richard B., Shi, Michael M., Kammerer, Stefan, Nelson, Matthew R., Stark, Mitchell S., Dumenil, Troy, Montgomery, Grant W., Hayward, Nicholas K., Martin, Nicholas G., Braun, Andreas and Duffy, David L. (2005) BRAF Polymorphisms and Risk of Melanocytic Neoplasia. Journal of Investigative Dermatology, 125 6: 1252-1258. doi:10.1111/j.0022-202X.2005.23937.x 50   16 Cited 17 times in Scopus17 0
Eri, R, Jonsson, JR, Pandeya, N, Purdie, DM, Clouston, AD, Martin, N, Duffy, D, Powell, EE, Fawcett, J, Florin, THJ and Radford-Smith, GL (2004) CCR5-Delta 32 mutation is strongly associated with primary sclerosing cholangitis. Genes And Immunity, 5 6: 444-450. doi:10.1038/sj.gene.6364113 412   34 Cited 45 times in Scopus45 1
Aitken, J., Welch, J., Duffy, D., Milligan, A., Green, A., Martin, N. G. and Hayward, N. (1999) CDKN2A variants in a population-based sample of Queensland families with melanoma. Journal of the National Cancer Institute, 91 5: 446-452. doi:10.1093/jnci/91.5.446 63   132 0
M. A. R. Ferreira, N. A. Oates, J. van Vliet, Z. Z. Zhao, M. Ehrich, N. G. Martin, G. W. Montgomery, E. Whitelaw and D. L. Duffy (2010) Characterization of the methylation patterns of MS4A2 in atopic cases and controls. ALLERGY, 65 3: 333-337. doi:10.1111/j.1398-9995.2009.02135.x 49   3 Cited 4 times in Scopus4 0
Kedda, MA, Shi, J, Duffy, D, Phelps, S, Yang, I, O'Hara, K, Fong, K and Thompson, PJ (2004) Characterization of two polymorphisms in the leukotriene C4 synthase gene in an Australian population of subjects with mild, moderate, and severe asthma. Journal of Allergy & Clinical Immunology, 113 5: 889-895. doi:10.1016/j.jaci.2004.02.008 65   45 Cited 49 times in Scopus49 0
Medland, S, Nyholt, D, Painter, JN, McEnvoy, BP, Allan McRae, Zhu, G, Gordon, SD, Ferreira, MAR, Wright, MJ, Henders, AK, Campbell MJ, Duffy, D, Hansell, N K, Macgregor, S, Slutske, WS, Heath, AC, Montgomery, GW and Martin, NG (2009) Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans. American Journal of Human Genetics, 85 5: 750-755. doi:10.1016/j.ajhg.2009.10.009 103   88 Cited 90 times in Scopus90 21
Banan, P., McClenahan, P., Duffy, D., Sturm, R. and Soyer, H. P. (2014). Dermoscopy, RCM and histopathology of a regressive melanoma in situ from an individual with a GSTP1 rs1695 polymorphism. In: The Australasian College of Dermatologists 47th Annual Scientific Meeting, Melbourne Australia, (27-27). 18–21 May 2014. doi:10.1111/ajd.12174 18   0 0
Liu, Fan, Wollstein, Andreas, Hysi, Pirro G., Ankra-Badu, Georgina A., Spector, Timothy D., Park, Daniel, Zhu, Gu, Larsson, Mats, Duffy, David L., Montgomery, Grant W., Mackey, David A., Walsh, Susan, Lao, Oscar, Hofman, Albert, Rivadeneira, Fernando, Vingerling, Johannes R., Uitterlinden, Andrew G., Martin, Nicholas G., Hammond, Christopher J. and Kayser, Manfred (2010) Digital quantification of human eye color highlights genetic association of three new loci. PLoS Genetics, 6 5: e1000934-1-e1000934-15. doi:10.1371/journal.pgen.1000934 83   48 Cited 57 times in Scopus57 23
Montgomery, Grant W., Zhao, Zhen Zehn, Morley, Katherine I., Marsh, Anna J., Boomsma, Dorret I., Martin, Nicholas G. and Duffy, David L. (2003) Dizygotic twinning is not associated with methylenetetrahydrofolate reductase haplotypes. Human Reproduction, 18 11: 2460-2464. doi:10.1093/humrep/deg441 44   10 Cited 11 times in Scopus11 0
Montgomery, Grant W., Duffy, David L., Hall, Jeff, Haddon, Barbara R., Kudo, Masataka, McGee, Elizabeth A., Palmer, James S., Hsueh, Aaron J., Boomsma, Dorrett I. and Martin, Nicholas G. (2000) Dizygotic Twinning Is Not Linked to Variation at the {alpha}-Inhibin Locus on Human Chromosome 2. Journal of Clinical Endocrinology & Metabolism, 85 9: 3391-3395. doi:10.1210/jc.85.9.3391 56   22 0
Hansell, N. K., James, M. R., Duffy, D. L., Birley, A. J., Luciano, M., Geffen, G. M., Wright, M. J., Montgomery, G. W. and Martin, N. G. (2007) Effect of the BDNF V166M polymorphism on working memory in healthy adolescents. Genes, Brain and Behavior, 6 3: 260-268. doi:10.1111/j.1601-183X.2006.00254.x 93   27 Cited 32 times in Scopus32 0
Whitfield, J. B., Cullen, L. M., Jazwinska, E. C., Powell, L. W., Heath, A. C., Zhu, Gu, Duffy, D. L. and Martin, N. G. (2000) Effects of HFE C282Y and H63D Polymorphisms and Polygenic Background on Iron Stores in a Large Community Sample of Twins. American Journal of Human Genetics, 66 4: 1246-1258. doi:10.1086/302862 136   109 Cited 113 times in Scopus113 0
Luciano, M, Hine, E., Wright, M. J., Duffy, D. L., MacMillan, J. and Martins, N. G. (2007) Effects of SCA1, MJD, and DPRLA triplet repeat polymorphisms on cognitive phenotypes in a normal population of adolescent twins. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 144B 1: 95-100. doi:10.1002/ajmg.b.30413 119   3 Cited 3 times in Scopus3 0
James, Michael R., Hayward, Nicholas K., Dumenil, Troy, Montgomery, Grant W., Martin, Nicholas G. and Duffy, David L. (2004) Epidermal Growth Factor Gene (EGF) Polymorphism and Risk of Melanocytic Neoplasiay. Journal of Investigative Dermatology, 123 4: 760-762. doi:10.1111/j.0022-202X.2004.23305.x 45   35 Cited 36 times in Scopus36 0
Anderson, Carl A., Duffy, David L., Martin, Nicholas G. and Visscher, Peter M. (2007) Estimation of variance components for age at menarche in twin families. Behavior Genetics, 37 5: 668-677. doi:10.1007/s10519-007-9163-2 68   30 Cited 29 times in Scopus29 0
Johnatty, Sharon E., Beesley, Jonathan, Chen, Xiaoqing, Macgregor, Stuart, Duffy, David L., Spurdle, Amanda B., deFazio, Anna, Gava, Natalie, Webb, Penelope M., Australian Ovarian Cancer Study Group, Australian Cancer Study (Ovarian Cancer), Rossing, Mary Anne, Doherty, Jennifer Anne, Goodman, Marc T., Lurie, Galina, Thompson, Pamela J., Wilkens, Lynne R., Ness, Roberta B., Moysich, Kirsten B., Chang-Claude, Jenny, Wang-Gohrke, Shan, Cramer, Daniel W., Terry, Kathryn L., Hankinson, Susan E., Tworoger, Shelley S., Garcia-Closas, Montserrat, Yang, Hannah, Lissowska, Jolanta, Chanock, Stephen J., Pharoah, Paul D., Song, Honglin, Whitemore, Alice S., Pearce, Celeste L., Stram, Daniel O., Wu, Anna H., Pike, Malcolm C., Gayther, Simon A., Ramus, Susan J., Menon, Usha, Gentry-Maharaj, Aleksandra, Anton-Culver, Hoda, Ziogas, Argyrios, Hogdall, Estrid, Kjaer, Susanne K., Hogdall, Claus, Berchuck, Andrew, Schildkraut, Joellen M., Iversen, Edwin S., Moorman, Patricia G., Phelan, Catherine M., Sellers, Thomas A., Cunningham, Julie M., Vierkant, Robert A., Rider David N., Goode, Ellen L., Haviv, Izhak, Chenevix-Trench, Georgia and Ovarian Cancer Association Consortium (2010) Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility "Hot-Spot". PLoS Genetics, 6 7: e1001016-1-e1001016-10. doi:10.1371/journal.pgen.1001016 115 1 29 Cited 22 times in Scopus22 3
Karihaloo, C., Tovey, E.R., Mitakakis, T.Z., Duffy, D.L. and Britton, W.J. (2002) Evidence for the genetic control of immunoglobulin E reactivity to the allergens of Alternaria alternata. Clinical And Experimental Allergy, 32 9: 1316-1322. doi:10.1046/j.1365-2745.2002.01447.x 60   7 Cited 9 times in Scopus9 0
Whitfield, John B., Dy, Veronica, McQuilty, Robert, Zhu, Gu, Montgomery, Grant W., Ferreira, Manuel A. R., Duffy, David L., Neale, Michael C., Heijmans, Bas T., Heath, Andrew C. and Martin, Nicholas G. (2007) Evidence of genetic effects on blood lead concentration. Environmental Health Perspectives, 115 8: 1224-1230. doi:10.1289/ehp.8847 80   12 Cited 10 times in Scopus10 0
Jeske, YW, So, A, Kelemen, L, Bulmer, B, Gordon, RD, Duffy, D and Stowasser, M (2007). Examination of candidate genes at chromosome 7p22 in familial hyperaldosteronism type II. In: Hypertension: Proceedings of the High Blood Pressure Research Council of Australia 2006 Annual Scientific Meeting. 28th Annual Scientific Meeting of the High Blood Pressure Research Council of Australia, Brisbane, Australia, (1469-1469). 7-8 December 2006. doi:10.1161/HYPERTENSIONAHA.107.009421 118   1 0
Jeske, Y., So, A., Kelemen, L, Sukor, N., Willys, C., Bulmer, B. J., Gordon, R. D., Duffy, D. and Stowasser, M. (2008). Examination of chromosome 7p22 candidate genes RBaK, PMS2 and GNA12 in familial hyperaldosteronism type II. In: W. P. Anderson, Clinical and Experimental Pharmacology and Physiology: Proceedings of IVth Franco-Australian Meeting on Hypertension. IVth Franco-Australian Meeting on Hypertension, Northern Territory, Australia, (380-385). September 2007. doi:10.1111/j.1440-1681.2008.04882.x 59   16 Cited 15 times in Scopus15 0
Thomsen, Simon Francia, van der Sluis, Sophie, Stensballe, Lone G, Posthuma, Danielle, Skytthe, Axel, Kyvik, Kirsten O, Duffy, David L, Backer, Vibeke and Bisgaard, Hans (2009) Exploring the association between severe respiratory syncytial virus infection and asthma: A registry-based twin study. American Journal of Respiratory and Critical Care Medicine, 179 12: 1091-1097. doi:10.1164/rccm.200809-1471OC 34   61 Cited 76 times in Scopus76 0
So, A., Stowasser, M., Gordon, R., Duffy, D. and Jeske, Y. (2005). Familial hyperaldosteronism type II (FH-II): Further evidence for linkage at chromosome 7p22 but also for the predicted genetic heterogeneity. In: Clinical and Experimental Pharmacology and Physiology: Abstract of the 26th Annual Scientific Meeting of the High Blood Pressure Research Council of Australia Inc.. The 26th Annual Scientific Meeting of the High Blood Pressure Research Council of Australia Inc., Sydney, Australia, (A24-A25). 24-26 November, 2004. 64   0
So, A, Duffy, DL, Gordon, RD, Jeske, YWA, Lin-Su, K, New, MI and Stowasser, M (2005) Familial hyperaldosteronism type II is linked to the chromosome 7p22 region but also shows predicted heterogeneity. Journal of Hypertension, 23 8: 1477-1484. doi:10.1097/01.hjh.0000174299.66369.26 77   43 Cited 48 times in Scopus48 0
Good, D, Busfield, F, Duffy, D, Lovelock, PK, Kesting, JB, Cameron, DP and Shaw, JTE (2001) Familial Paget's disease of bone: Nonlinkage to the PDB1 and PDB2 loci on chromosomes 6p and 18q in a large pedigree. Journal of Bone And Mineral Research, 16 1: 33-38. doi:10.1359/jbmr.2001.16.1.33 122   23 0
Good, David, FRANCES BUSFIELD, Duffy, David, PAUL K. LOVELOCK, JANINE B. KESTING, DONALD P. CAMERON and Shaw, Joanne (2001) Familial Paget's Disease of Bone: Nonlinkage to the PDB1 and PDB2 Loci on Chromosomes 6p and 18q in a Large Pedigree. Journal of Bone and Mineral Research, 16 1: 33-38. doi:10.1359/jbmr.2001.16.1.33 55   23 0
E. M. Byrne, A. F. McRae, D. L. Duffy, Z. Z. Zhao, N. G. Martin, J. B. Whitfield, P. M. Visscher and G. W. Montgomery (2009) Family-based mitochondrial association study of traits related to type 2 diabetes and the metabolic syndrome in adolescents. Diabetologia, 52 11: 2359-2368. doi:10.1007/s00125-009-1510-9 43   2 Cited 3 times in Scopus3 0
Sukor, Norlela, Mulatero, Paolo, Gordon, Richard D., So, Albertina, Duffy, David, Bertello, Chiara, Kelemen, Livia, Jeske, Yvette, Veglio, Franco and Stowasser, Michael (2008) Further evidence for linkage of familial hyperaldosteronism type II at chromosome 7p22 in Italian as well as Australian and South American families. Journal of Hypertension, 26 8: 1577-1582. doi:10.1097/HJH.0b013e3283028352 55   27 Cited 35 times in Scopus35 3
So, Albertina, Stowasser, Michael, Gordon, Richard, Duffy, David and Jeske, Yvette (2005). Further evidence of linkage at 7p22 with familial hyperaldosteronism type II. In: NPG, American Journal of Hypertension. 20th Annual Scientific Meeting of the American Society of Hypertension, San Francisco, USA, (A240-A240). 14-18 May 2005. doi:10.1016/j.amjhyper.2005.03.659 45   0 0

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