Hasil Pencarian - Adam D. McIntyre

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  1. 1
    Complex genetic architecture in severe hypobetalipoproteinemia

    Complex genetic architecture in severe hypobetalipoproteinemia oleh Linda R. Wang, Adam D. McIntyre, Robert A. Hegele

    Diterbitkan 2018-03-01
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  2. 2
    Reduced lipoprotein (a) in patients with severe hypertriglyceridaemia

    Reduced lipoprotein (a) in patients with severe hypertriglyceridaemia oleh Erin O. Jacob, Adam D. McIntyre, Jian Wang, Robert A. Hegele

    Diterbitkan 2024-10-01
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  3. 3
    Whole-exome sequencing identifies a novel insertion in an Ontario family with brachydactyly type A1

    Whole-exome sequencing identifies a novel insertion in an Ontario family with brachydactyly type A1 oleh Rosettia Ho, Adam D McIntyre, Brooke A Kennedy, Robert A Hegele

    Diterbitkan 2018-12-01
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  4. 4
    Lipoprotein(a) in Familial Hypercholesterolemia

    Lipoprotein(a) in Familial Hypercholesterolemia oleh Erin O. Jacob, BMSc, Adam D. McIntyre, BSc, Jian Wang, MD, Robert A. Hegele, MD

    Diterbitkan 2024-01-01
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  5. 5
    Carotid intima-medial thickness in patients with severe hypertriglyceridemia

    Carotid intima-medial thickness in patients with severe hypertriglyceridemia oleh Maud Ahmad, Brooke A. Kennedy, Surim Son, Adam D. McIntyre, Julieta Lazarte, Jian Wang, Robert A. Hegele

    Diterbitkan 2024-06-01
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  6. 6
    Use of next-generation sequencing to detect LDLR gene copy number variation in familial hypercholesterolemia

    Use of next-generation sequencing to detect LDLR gene copy number variation in familial hypercholesterolemia oleh Michael A. Iacocca, Jian Wang, Jacqueline S. Dron, John F. Robinson, Adam D. McIntyre, Henian Cao, Robert A. Hegele

    Diterbitkan 2017-11-01
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  7. 7
    Severe Combined Dyslipidemia With a Complex Genetic Basis

    Severe Combined Dyslipidemia With a Complex Genetic Basis oleh Ryan Le MD, Minan Abbas MB ChB, FRCPC, Adam D. McIntyre BSc, Robert A. Hegele MD, FRCPC, FACP

    Diterbitkan 2019-09-01
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  8. 8
    Six years’ experience with LipidSeq: clinical and research learnings from a hybrid, targeted sequencing panel for dyslipidemias

    Six years’ experience with LipidSeq: clinical and research learnings from a hybrid, targeted sequencing panel for dyslipidemias oleh Jacqueline S. Dron, Jian Wang, Adam D. McIntyre, Michael A. Iacocca, John F. Robinson, Matthew R. Ban, Henian Cao, Robert A. Hegele

    Diterbitkan 2020-02-01
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  9. 9
    A De Novo Mutation Associated With Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome in a Family With Werner Syndrome

    A De Novo Mutation Associated With Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome in a Family With Werner Syndrome oleh Linda R. Wang MD, Aleksandar Radonjic BSc, Allison A. Dilliott BSc, Adam D. McIntyre BSc, Robert A. Hegele MD, FRCPC, FACP

    Diterbitkan 2018-07-01
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  10. 10
    Genetic Determinants of Myocardial Infarction Risk in Familial Hypercholesterolemia

    Genetic Determinants of Myocardial Infarction Risk in Familial Hypercholesterolemia oleh Pei Jun Zhao, MD, Matthew R. Ban, BSc, Michael A. Iacocca, MSc, Adam D. McIntyre, BSc, Jian Wang, MD, Robert A. Hegele, MD

    Diterbitkan 2019-09-01
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  11. 11
    LipidSeq: a next-generation clinical resequencing panel for monogenic dyslipidemias[S]

    LipidSeq: a next-generation clinical resequencing panel for monogenic dyslipidemias[S] oleh Christopher T. Johansen, Joseph B. Dubé, Melissa N. Loyzer, Austin MacDonald, David E. Carter, Adam D. McIntyre, Henian Cao, Jian Wang, John F. Robinson, Robert A. Hegele

    Diterbitkan 2014-04-01
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  12. 12
    Abetalipoproteinemia Due to a Novel Splicing Variant in in 3 Siblings

    Abetalipoproteinemia Due to a Novel Splicing Variant in in 3 Siblings oleh Caitlyn Vlasschaert MD, MSc, Adam D. McIntyre BSc, Lauren A. Thomson BSc, Brooke A. Kennedy BSc, Suzanne Ratko RD, Chitra Prasad MD, FRCPC, FCCMG, Robert A. Hegele MD, FRCPC, FACP

    Diterbitkan 2021-06-01
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  13. 13
    The apolipoprotein C-III (Gln38Lys) variant associated with human hypertriglyceridemia is a gain-of-function mutation

    The apolipoprotein C-III (Gln38Lys) variant associated with human hypertriglyceridemia is a gain-of-function mutation oleh Meenakshi Sundaram, Kaitlin R. Curtis, Mohsen Amir Alipour, Nicholas D. LeBlond, Kaitlyn D. Margison, Rebecca A. Yaworski, Robin J. Parks, Adam D. McIntyre, Robert A. Hegele, Morgan D. Fullerton, Zemin Yao

    Diterbitkan 2017-11-01
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  14. 14
    Partial LPL deletions: rare copy-number variants contributing towards severe hypertriglyceridemia

    Partial LPL deletions: rare copy-number variants contributing towards severe hypertriglyceridemia oleh Jacqueline S. Dron, Jian Wang, Adam D. McIntyre, Henian Cao, John F. Robinson, P. Barton Duell, Priya Manjoo, James Feng, Irina Movsesyan, Mary J. Malloy, Clive R. Pullinger, John P. Kane, Robert A. Hegele

    Diterbitkan 2019-11-01
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  15. 15
    Polygenic determinants in extremes of high-density lipoprotein cholesterol

    Polygenic determinants in extremes of high-density lipoprotein cholesterol oleh Jacqueline S. Dron, Jian Wang, Cécile Low-Kam, Sumeet A. Khetarpal, John F. Robinson, Adam D. McIntyre, Matthew R. Ban, Henian Cao, David Rhainds, Marie-Pierre Dubé, Daniel J. Rader, Guillaume Lettre, Jean-Claude Tardif, Robert A. Hegele

    Diterbitkan 2017-11-01
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  16. 16
    Contribution of rare variant associations to neurodegenerative disease presentation

    Contribution of rare variant associations to neurodegenerative disease presentation oleh Allison A. Dilliott, Abdalla Abdelhady, Kelly M. Sunderland, Sali M. K. Farhan, Agessandro Abrahao, Malcolm A. Binns, Sandra E. Black, Michael Borrie, Leanne K. Casaubon, Dar Dowlatshahi, Elizabeth Finger, Corinne E. Fischer, Andrew Frank, Morris Freedman, David Grimes, Ayman Hassan, Mandar Jog, Sanjeev Kumar, Donna Kwan, Anthony E. Lang, Jennifer Mandzia, Mario Masellis, Adam D. McIntyre, Stephen H. Pasternak, Bruce G. Pollock, Tarek K. Rajji, Ekaterina Rogaeva, Demetrios J. Sahlas, Gustavo Saposnik, Christine Sato, Dallas Seitz, Christen Shoesmith, Thomas D. L. Steeves, Richard H. Swartz, Brian Tan, David F. Tang-Wai, Maria C. Tartaglia, John Turnbull, Lorne Zinman, ONDRI Investigators, Robert A. Hegele

    Diterbitkan 2021-09-01
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