Rezultati - Joan E. Bailey‐Wilson
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Genomewide Linkage Scan for Myopia Susceptibility Loci among Ashkenazi Jewish Families Shows Evidence of Linkage on Chromosome 22q12 od Dwight Stambolian, Grace Ibay, Lauren Reider, Debra Dana, Chris Moy, Melissa Schlifka, Taura N. Holmes, Elise Ciner, Joan E. Bailey‐Wilson
Izdano 2004Artigo -
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Attention-Deficit/Hyperactivity Disorder in a Population Isolate: Linkage to Loci at 4q13.2, 5q33.3, 11q22, and 17p11 od Mauricio Arcos‐Burgos, F. Xavier Castellanos, David Pineda, Francisco Lopera, Juan David Palacio, Luis Palacio, Judith L. Rapoport, Kate Berg, Joan E. Bailey‐Wilson, Maximilian Muenke
Izdano 2004Artigo -
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Determination of the allelic frequency in Smith–Lemli–Opitz syndrome by analysis of massively parallel sequencing data sets od Jennifer L. Cross, James Iben, Claire L. Simpson, Audrey Thurm, Susan E. Swedo, Elaine Tierney, Joan E. Bailey‐Wilson, Leslie G. Biesecker, Forbes D. Porter, Christopher A. Wassif
Izdano 2014Artigo -
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High incidence of unrecognized visceral/neurological late-onset Niemann-Pick disease, type C1, predicted by analysis of massively parallel sequencing data sets od Christopher A. Wassif, Joanna Cross, James Iben, Luis Sánchez‐Pulido, Antony Cougnoux, Frances M. Platt, Daniel S. Ory, Chris P. Ponting, Joan E. Bailey‐Wilson, Leslie G. Biesecker, Forbes D. Porter
Izdano 2015Artigo -
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Assessing the Genetic Predisposition of Education on Myopia: A Mendelian Randomization Study od Gabriel Cuéllar-Partida, Yi Lu, Pik Fang Kho, Alex W. Hewitt, H.‐Erich Wichmann, Seyhan Yazar, Dwight Stambolian, Joan E. Bailey‐Wilson, Robert Wojciechowski, Jie Jin Wang, Paul Mitchell, David A. Mackey, Stuart MacGregor
Izdano 2015Artigo -
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A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1 od Ying Chen, Melissa A. Gilbert, Christopher M. Grochowski, Deborah McEldrew, Jessica Llewellyn, Orith Waisbourd‐Zinman, Hákon Hákonarson, Joan E. Bailey‐Wilson, Pierre Russo, Rebecca G. Wells, Kathleen M. Loomes, Nancy B. Spinner, Marcella Devoto
Izdano 2018Artigo -
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Hereditary nonpolyposis colorectal cancer (lynch syndromes I and II). II. Biomarker studies od Henry T. Lynch, Guy S. Schuelke, William J. Kimberling, William A. Albano, Jane F. Lynch, Karen A. Biscone, Martin Lipkin, Eleanor E. Deschner, Yves B. Mikol, Avery A. Sandberg, Robert C. Elston, Joan E. Bailey‐Wilson, B. Shannon Danes
Izdano 1985Artigo -
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Germline Alterations of the RNASEL Gene, a Candidate HPC1 Gene at 1q25, in Patients and Families with Prostate Cancer od Annika Rökman, Tarja Ikonen, Eija H. Seppälä, Nina N. Nupponen, Ville Autio, Nina Mononen, Joan E. Bailey‐Wilson, Jeffrey M. Trent, John D. Carpten, Mika Matikainen, Pasi A. Koivisto, Teuvo L.J. Tammela, Olli Kallioniemi, Johanna Schleutker
Izdano 2002Artigo
Iskalna orodja:
Sorodne teme
Biology
Gene
Genetics
Medicine
Genotype
Single-nucleotide polymorphism
Internal medicine
Allele
Genetic linkage
Cancer
Genome-wide association study
Locus (genetics)
Mutation
Oncology
Genetic association
Population
Environmental health
Computational biology
Disease
Lung cancer
Mathematics
Phenotype
Prostate cancer
Computer science
Haplotype
Pathology
Refractive error
Exome sequencing
Genome
Germline mutation