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Results: 1-11 |
Results: 11

Authors: Weeks, Daniel E. Conley, Yvette P. Tsai, Hui-Ju Mah, Tammy S. Schmidt, Silke Poste, Eric A. Agarwal, Anita Haines, Jonathan L. Pericak-Vance, Margaret A. Rosenfeld, Philip J. Paul, T. Otis Eller, Andrew W. Morse, Lawrence S. Dailey, J.P. Ferrell, Robert E. Gorin, Michael B.
Citation: E. Weeks, Daniel et al., Age-Related Maculopathy: A Genomewide Scan with Continued Evidence of Susceptibility Loci within the 1q31, 10q26, and 17q25 Regions, American journal of human genetics , 75(2), 2004, pp. 174-189

Authors: Rouleau, Guy A. Seizinger, Bernd R. Wertelecki, Wladimir Haines, Jonathan L. Superneau, Duane W. Martuza, Robert L. Gusella, lames F.
Citation: A. Rouleau, Guy et al., Flanking markers bracket the neurofibromatosis type 2 (NF2) gene on chromosome 22, American journal of human genetics , 46-I(2), 1990, pp. 323-328

Authors: Hauser, Elizabeth R. Crossman, David C. Granger, Christopher B. Haines, Jonathan L. Jones, Christopher J.H. Mooser, Vincent McAdam, Brendan Winkelmann, Bernhard R. Wiseman, Alan H. Muhlestein, J. Brent Bartel, Alan G. Dennis, Charles A. Dowdy, Elaine Estabrooks, Susan Eggleston, Karen Francis, Sheila Roche, Kath Clevenger, Paula W. Huang, Liling Pedersen, Bonnie Shah, Svati Schmidt, Silke Haynes, Carol West, Sandra Asper, Donny Booze, Michael Sharma, Sanjay Sundseth, Scott Middleton, Lefkos Roses, Allen D. Hauser, Michael A. Vance, Jeffrey M. Pericak-Vance, Margaret A. Kraus, William E:
Citation: R. Hauser, Elizabeth et al., A Genomewide Scan for Early-Onset Coronary Artery Disease in 438 Families: The GENECARD Study, American journal of human genetics , 75(3), 2004, pp. 436-447

Authors: Tanzi, Rudolph E. Watkins, Paul C. Stewart, Gordon D. Wexler, Nancy S. Gusella, James F. Haines, Jonathan L.
Citation: E. Tanzi, Rudolph et al., A genetic linkage map of human chromosome 21: analysis of recombination as a function of sex and age., American journal of human genetics , 50-I(3), 1992, pp. 551-558

Authors: Wang, Liyong Hauser, Elizabeth R. Shah, Svati H. Pericak-Vance, Margaret A. Haynes, Carol Crosslin, David Harris II, Marco Nelson, Sarah Hale, A. Brent Granger, Christopher B. Haines, Jonathan L. Jones, Christopher J.H. Crossman, David Seo, David Gregory, Simon G. Kraus, William E. Goldschmidt-Clermont, Pascal J. Vance, Jeffery M.
Citation: Wang, Liyong et al., Peakwide Mapping on Chromosome 3q13 Identifies the Kalirin Gene as a Novel Candidate Gene for Coronary Artery Disease, American journal of human genetics , 80(4), 2007, pp. 650-663

Authors: Haines, Jonathan L. Short, M. Priscilla Kwiatkowski, David J. Jewell, Ann Andermann, Eva Bejjani, Bassem Yang, Ching-Hwa Gusella, James F. Amos, Jean A.
Citation: L. Haines, Jonathan et al., Localization of one gene for tuberous sclerosis within 9q32-9q34, and further evidence for heterogeneity., American journal of human genetics , 49-II(4), 1991, pp. 764-772

Authors: Walt, Joelle M. , Van: der Nicodemus, Kristin K. Martin, Eden R. Scott, William K. Nance, Martha A. Watts, Ray L. Hubble, Jean P. Haines, Jonathan L. Koller, William C. Lyons, Kelly Pahwa, Rajesh Stern, Matthew B. Colcher, Amy Hiner, Bradley C. Jankovic, Joseph Ondo, William G. Allen, Fred H. , Jr. Goetz, Chistopher G. Small, Gary W. Mastaglia, Frank Stajich, Jeffrey M. McLaurin, Adam C. Middleton, Lefkos T. Scott, Burton L. Schmechel, Donald E. Pericak-Vance, Margaret A. Vance, Jeffrey M.
Citation: Walt, Joelle M. , Van: Der et al., Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease, American journal of human genetics , 72(4), 2003, pp. 804-811

Authors: Schmidt, Silke Hauser, Michael A Scott, William K Postel, Eric A. Agarwal, Anita Gallins, Paul Wong, Frank Chen, Yu Sarah Spencer, Kylee Schnetz-Boutaud, Nathalie Haines, Jonathan L. Pericak-Vance, Margaret A.
Citation: Schmidt, Silke et al., Cigarette Smoking Strongly Modifies the Association of LOC387715 and Age-Related Macular Degeneration, American journal of human genetics , 78(5), 2006, pp. 852-864

Authors: McClatchey, Andrea I. Trofatter, James McKenna-Yasek, Diane Raskind, Wendy Bird, Thomas Pericak-Vance, Margaret Gilchrist, James Arahata, Kiichi Radosavljevic, Danica Worthen, Hilary G. Van den Bergh, Peter Haines, Jonathan L. Gusella, James F. Brown, Robert H.
Citation: I. Mcclatchey, Andrea et al., Dinucleotide repeat polymorphisms at the SCN4A locus suggest allelic heterogeneity of hyperkalemic periodic paralysis and paramyotonia congenita, American journal of human genetics , 50-II(5), 1992, pp. 896-901

Authors: Scott, William K. Hauser, Elizabeth R. Schmechel, Donald E. Welsh-Bohmer, Kathleen A. Small, Gary W. Roses, Allen D. Saunders, Ann M. Gibert, John R. Vance, Jeffrey M. Haines, Jonathan L. Pericak-Vance, Margaret A.
Citation: K. Scott, William et al., Ordered-Subsets Linkage Analysis Detects Novel Alzheimer Disease Loci on Chromosomes 2q34 and 15q22, American journal of human genetics , 73(5), 2003, pp. 1041-1051

Authors: Ionasescu, Victor V. Trofatter, James Haines, Jonathan L. Summers, Anne M. Ionasescu, Rebecca Searby, Charles
Citation: V. Ionasescu, Victor et al., Heterogeneity in X-linked recessive Charcot-Marie-Tooth neuropathy., American journal of human genetics , 48-II(6), 1991, pp. 1075-1083
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