Výsledky vyhledávání - Yee Him Cheung

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  1. 1
    Whole-Exome sequencing identifies novel<i>LEPR</i>mutations in individuals with severe early onset obesity

    Whole-Exome sequencing identifies novel<i>LEPR</i>mutations in individuals with severe early onset obesity Autor Richard Gill, Yee Him Cheung, Yufeng Shen, Patricia Lanzano, Nazrat Mirza, Svetlana Ten, Noel K. Maclaren, Roja Motaghedi, Joan C. Han, Jack A. Yanovski, Rudolph L. Leibel, Wendy K. Chung

    Vydáno 2013
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  2. 2
    Variants in GATA4 are a rare cause of familial and sporadic congenital diaphragmatic hernia

    Variants in GATA4 are a rare cause of familial and sporadic congenital diaphragmatic hernia Autor Lan Yu, Julia Wynn, Yee Him Cheung, Yufeng Shen, George B. Mychaliska, Timothy M. Crombleholme, Kenneth S. Azarow, Foong‐Yen Lim, Dai H. Chung, Douglas A. Potoka, Brad W. Warner, Brian T. Bucher, Charles J.H. Stolar, Guðrún Aspelund, Marc S. Arkovitz, Wendy K. Chung

    Vydáno 2012
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  3. 3
    Whole exome sequencing identifies de novo mutations in<i>GATA6</i>associated with congenital diaphragmatic hernia

    Whole exome sequencing identifies de novo mutations in<i>GATA6</i>associated with congenital diaphragmatic hernia Autor Lan Yu, James T. Bennett, Julia Wynn, Gemma L. Carvill, Yee Him Cheung, Yufeng Shen, George B. Mychaliska, Kenneth S. Azarow, Timothy M. Crombleholme, Dai H. Chung, Douglas A. Potoka, Brad W. Warner, Brian T. Bucher, Foong‐Yen Lim, John B. Pietsch, Charles J.H. Stolar, Guðrún Aspelund, Marc S. Arkovitz, Heather C. Mefford, Wendy K. Chung

    Vydáno 2014
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  4. 4
    A Recurrent PDGFRB Mutation Causes Familial Infantile Myofibromatosis

    A Recurrent PDGFRB Mutation Causes Familial Infantile Myofibromatosis Autor Yee Him Cheung, Tenzin Gayden, Philippe M. Campeau, Charles A. LeDuc, Donna Russo, Văn Hùng Nguyễn, Jiancheng Guo, Ming Qi, Yanfang Guan, Steffen Albrecht, Brenda Moroz, Karen W. Eldin, James T. Lu, Jeremy Schwartzentruber, David Malkin, Albert M. Berghuis, Sherif Emil, Richard A. Gibbs, David L. Burk, Megan R. Vanstone, Brendan Lee, David Orchard, Kym M. Boycott, Wendy K. Chung, Nada Jabado

    Vydáno 2013
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  5. 5
    De novo mutations in histone-modifying genes in congenital heart disease

    De novo mutations in histone-modifying genes in congenital heart disease Autor Samir Zaidi, Murim Choi, Hiroko Wakimoto, Lijiang Ma, Jianming Jiang, John D. Overton, Angela Romano-Adesman, Robert Bjornson, Roger E. Breitbart, Kerry K. Brown, Nicholas Carriero, Yee Him Cheung, John Deanfield, Steven R. DePalma, Khalid A. Fakhro, Joseph Glessner, Hákon Hákonarson, Michael J. Italia, Jonathan R. Kaltman, Juan Pablo Kaski, Richard Kim, Jennie Kline, Teresa Lee, Jeremy Leipzig, Alexander Lopez, Shrikant Mane, Laura E. Mitchell, Jane W. Newburger, Michael Parfenov, Itsik Pe’er, George A. Porter, Amy E. Roberts, Ravi Sachidanandam, Stephan Sanders, Howard Seiden, Matthew W. State, Sai Lakshmi Subramanian, Irina R. Tikhonova, Wei Wang, Dorothy Warburton, Peter S. White, Ismée A. Williams, Hongyu Zhao, Jonathan G. Seidman, Martina Brueckner, Wendy K. Chung, Bruce D. Gelb, Elizabeth Goldmuntz, Christine E. Seidman, Richard P. Lifton

    Vydáno 2013
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