Sökresultat - Mark Leppert

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  1. 1
    Cytogenetic and molecular studies of trisomy 13.

    Cytogenetic and molecular studies of trisomy 13. av Terry Hassold, P. A. Jacobs, Mark Leppert, Michael Sheldon

    Publicerad 1987
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  2. 2
    The Spectrum of Symptoms and QT Intervals in Carriers of the Gene for the Long-QT Syndrome

    The Spectrum of Symptoms and QT Intervals in Carriers of the Gene for the Long-QT Syndrome av G. Michael Vincent, Katherine W. Timothy, Mark Leppert, Mark Keating

    Publicerad 1992
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  3. 3
    Bloom syndrome: an analysis of consanguineous families assigns the locus mutated to chromosome band 15q26.1.

    Bloom syndrome: an analysis of consanguineous families assigns the locus mutated to chromosome band 15q26.1. av J German, Anne Marie Roe, Mark Leppert, Nathan A. Ellis

    Publicerad 1994
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  4. 4
    BAT-26 and BAT-40 Instability in Colorectal Adenomas and Carcinomas and Germline Polymorphisms

    BAT-26 and BAT-40 Instability in Colorectal Adenomas and Carcinomas and Germline Polymorphisms av Wade S. Samowitz, Martha L. Slattery, John D. Potter, Mark Leppert

    Publicerad 1999
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  5. 5
    Genome Scans for Blood Pressure and Hypertension

    Genome Scans for Blood Pressure and Hypertension av Steven C. Hunt, R. Curtis Ellison, Larry D. Atwood, James S. Pankow, Michael A. Province, Mark Leppert

    Publicerad 2002
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  6. 6
    A human vascular disorder, supravalvular aortic stenosis, maps to chromosome 7.

    A human vascular disorder, supravalvular aortic stenosis, maps to chromosome 7. av A K Ewart, C. A. Morris, Greg Ensing, James Loker, Cynthia A. Moore, Mark Leppert, Mark Keating

    Publicerad 1993
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  7. 7
    Prognostic significance of <i>p53</i> mutations in colon cancer at the population level

    Prognostic significance of <i>p53</i> mutations in colon cancer at the population level av Wade S. Samowitz, Karen Curtin, Khe-Ni Ma, Sandra L. Edwards, Donna Schaffer, Mark Leppert, Martha L. Slattery

    Publicerad 2002
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  8. 8
    Identification of Rare Recurrent Copy Number Variants in High-Risk Autism Families and Their Prevalence in a Large ASD Population

    Identification of Rare Recurrent Copy Number Variants in High-Risk Autism Families and Their Prevalence in a Large ASD Population av Nori Matsunami, Dexter Hadley, Charles H. Hensel, G. Bryce Christensen, Cecilia Kim, Edward C. Frackelton, Kelly Thomas, Renata Pellegrino da Silva, Jeff Stevens, Lisa Baird, Brith Otterud, Karen S. Ho, Tena Varvil, Mark Leppert, Christophe G Lambert, Mark Leppert, Hákon Hákonarson

    Publicerad 2013
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  9. 9
    Novel Locus for Autosomal Dominant Hereditary Spastic Paraplegia, on Chromosome 8q

    Novel Locus for Autosomal Dominant Hereditary Spastic Paraplegia, on Chromosome 8q av Peter Hedera, Shirley Rainier, David M. Alvarado, Xinping Zhao, J Williamson, Brith Otterud, Mark Leppert, John K. Fink

    Publicerad 1999
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  10. 10
    Demonstration of Protein-Based Human Identification Using the Hair Shaft Proteome

    Demonstration of Protein-Based Human Identification Using the Hair Shaft Proteome av Glendon J. Parker, Mark Leppert, Deon S. Anex, Jonathan K. Hilmer, Nori Matsunami, Lisa Baird, Jeffery Stevens, Krishna Parsawar, Blythe Durbin‐Johnson, David M. Rocke, Chad Nelson, Daniel J. Fairbanks, A. S. Wilson, Robert H. Rice, Scott R. Woodward, Brian Bothner, Bradley R. Hart, Mark Leppert

    Publicerad 2016
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  11. 11
    Quantitative-Trait Loci Influencing Body-Mass Index Reside on Chromosomes 7 and 13: The National Heart, Lung, and Blood Institute Family Heart Study

    Quantitative-Trait Loci Influencing Body-Mass Index Reside on Chromosomes 7 and 13: The National Heart, Lung, and Blood Institute Family Heart Study av Mary F. Feitosa, Ingrid B. Borecki, Stephen S. Rich, Donna K. Arnett, Phyliss Sholinsky, Richard H. Myers, Mark Leppert, Michael A. Province

    Publicerad 2002
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  12. 12
    Replication of Linkage of Familial Combined Hyperlipidemia to Chromosome 1q With Additional Heterogeneous Effect of Apolipoprotein A-I/C-III/A-IV Locus

    Replication of Linkage of Familial Combined Hyperlipidemia to Chromosome 1q With Additional Heterogeneous Effect of Apolipoprotein A-I/C-III/A-IV Locus av Hilary Coon, Richard H. Myers, Ingrid B. Borecki, Donna K. Arnett, Steven C. Hunt, Michael A. Province, Luc Djoussé, Mark Leppert

    Publicerad 2000
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  13. 13
    Genetic Mapping of Ossification of the Posterior Longitudinal Ligament of the Spine

    Genetic Mapping of Ossification of the Posterior Longitudinal Ligament of the Spine av Hiroaki Koga, Takashi Sakou, Eiji Taketomi, Kyouji Hayashi, Takuya Numasawa, Seiko Harata, Kazunori Yone, Shunji Matsunaga, Brith Otterud, Ituro Inoue, Mark Leppert

    Publicerad 1998
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  14. 14
    The colon cancer burden of genetically defined hereditary nonpolyposis colon cancer

    The colon cancer burden of genetically defined hereditary nonpolyposis colon cancer av Wade S. Samowitz, Karen Curtin, Heather H. Lin, Margaret Robertson, Donna Schaffer, Melanie F. Nichols, Kristen M. Gruenthal, Mark Leppert, Martha L. Slattery

    Publicerad 2001
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  15. 15
    Genetic Analysis of an Inherited Predisposition to Colon Cancer in a Family with a Variable Number of Adenomatous Polyps

    Genetic Analysis of an Inherited Predisposition to Colon Cancer in a Family with a Variable Number of Adenomatous Polyps av Mark Leppert, Randall W. Burt, Jaime Hughes, Wade S. Samowitz, Yusuke Nakamura, Scott R. Woodward, Eldon J. Gardner, Jean‐Marc Lalouel, R. White

    Publicerad 1990
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  16. 16
    Leukemia-associated minor histocompatibility antigen discovery using T-cell clones isolated by in vitro stimulation of naive CD8+ T cells

    Leukemia-associated minor histocompatibility antigen discovery using T-cell clones isolated by in vitro stimulation of naive CD8+ T cells av Marie Bleakley, Brith Otterud, Julia Richardt, Audrey D. Mollerup, Michael Hudecek, Tetsuya Nishida, Colette Chaney, Edus H. Warren, Mark Leppert, Stanley R. Riddell

    Publicerad 2010
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  17. 17
    Common variant of human NEDD4L activates a cryptic splice site to form a frameshifted transcript

    Common variant of human NEDD4L activates a cryptic splice site to form a frameshifted transcript av Diane M. Dunn, Tomoaki Ishigami, James S. Pankow, Andrew von Niederhausern, Jonathan K. Alder, Steven C. Hunt, Mark Leppert, J.-M. Lalouel, Robert B. Weiss

    Publicerad 2002
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  18. 18
    Toward targeting B cell cancers with CD4+ CTLs: identification of a CD19-encoded minor histocompatibility antigen using a novel genome-wide analysis

    Toward targeting B cell cancers with CD4+ CTLs: identification of a CD19-encoded minor histocompatibility antigen using a novel genome-wide analysis av Robbert M. Spaapen, Henk M. Lokhorst, Kelly van den Oudenalder, Brith Otterud, Harry Dolstra, Mark Leppert, Monique C. Minnema, Andries C. Bloem, Tuna Mutis

    Publicerad 2008
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  19. 19
    Exome Analysis of a Family With Pleiotropic Congenital Heart Disease

    Exome Analysis of a Family With Pleiotropic Congenital Heart Disease av Cammon B. Arrington, Steven B. Bleyl, Norisada Matsunami, Gabriel D. Bonnell, Brith Otterud, Douglas C. Nielsen, Jeffrey Stevens, Shawn Levy, Mark Leppert, Neil E. Bowles

    Publicerad 2012
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  20. 20
    Linkage of a familial platelet disorder with a propensity to develop myeloid malignancies to human chromosome 21q22.1-22.2

    Linkage of a familial platelet disorder with a propensity to develop myeloid malignancies to human chromosome 21q22.1-22.2 av Carolyn Y. Ho, Brith Otterud, RD Legare, Tena Varvil, Ruchi Saxena, DB DeHart, SE Kohler, JC Aster, S. Bruce Dowton, FP Li, Mark Leppert, DG Gilliland

    Publicerad 1996
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