Որոնման արդյունքները - Tracey Oh
- Ցուցադրվում են 1 - 3 արդյունքները 3
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1
The genotypic and phenotypic spectrum of PIGA deficiency Maja Tarailo‐Graovac, Graham Sinclair, Sylvia Stöckler‐Ipsiroglu, Margot Van Allen, Jacob Rozmus, Casper Shyr, Roberta Biancheri, Tracey Oh, Bryan Sayson, Mirafe Lafek, Colin J.D. Ross, Wendy P. Robinson, Wyeth W. Wasserman, Andrea Rossi, Clara DM van Karnebeek
Հրապարակվել է 2015Artigo -
2
Mutations in ILK, encoding integrin-linked kinase, are associated with arrhythmogenic cardiomyopathy Andreas Brodehl, Saman Rezazadeh, Tatjana Williams, Nicole Munsie, Daniel Liedtke, Tracey Oh, Raechel A. Ferrier, Yaoqing Shen, Steven J.M. Jones, Amy L. Stiegler, Titus J. Boggon, Henry J. Duff, Jan M. Friedman, William T. Gibson, Sarah J. Childs, Brenda Gerull
Հրապարակվել է 2019Artigo -
3
Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling Brett V. Johnson, Raman Kumar, Sabrina Oishi, Suzy Alexander, Maria Kasherman, Michelle Sanchez Vega, Atma M. Ivancevic, Alison Gardner, Deepti Domingo, Mark Corbett, Euan Parnell, Sehyoun Yoon, Tracey Oh, Matthew A. Lines, Henrietta Lefroy, Usha Kini, Margot Van Allen, Sabine Grønborg, Sandra Mercier, Sébastien Küry, Stéphane Bézieau, Laurent Pasquier, Martine Raynaud, Alexandra Afenjar, Thierry Billette de Villemeur, Boris Keren, Julie Désir, Lionel Van Maldergem, Martina Marangoni, Nicola Dikow, David A. Koolen, Peter M. VanHasselt, Marjan M. Weiss, Petra Zwijnenburg, Joaquim Sá, C Reis, Carlos López-Otı́n, Olaya Santiago‐Fernández, Alberto Fernández‐Jaén, Anita Rauch, Katharina Steindl, Pascal Joset, Amy Goldstein, Suneeta Madan‐Khetarpal, Elena Infante, Elaine H. Zackai, Carey McDougall, Vinodh Narayanan, Keri Ramsey, Saadet Mercimek‐Andrews, Loren D.M. Peña, Vandana Shashi, Kelly Schoch, Jennifer A. Sullivan, Filippo Pinto e Vairo, Pavel N. Pichurin, Sarah Ewing, Sarah Barnett, Eric W. Klee, Matthew Perry, Mary Kay Koenig, Catherine E. Keegan, Jane L. Schuette, Stephanie Asher, Yezmin Perilla‐Young, Laurie D. Smith, Jill A. Rosenfeld, Elizabeth Bhoj, Paige Kaplan, Dong Li, Renske Oegema, Ellen van Binsbergen, Bert van der Zwaag, Marie Falkenberg Smeland, Ioana Cutcutache, Matthew Page, Martin Armstrong, Angela E. Lin, Marcie Steeves, Nicolette S. den Hollander, Mariëtte J.V. Hoffer, Margot R.F. Reijnders, Serwet Demirdas, Daniel C. Koboldt, Dennis Bartholomew, Theresa Mihalic Mosher, Scott E. Hickey, Christine Shieh, Pedro A. Sanchez‐Lara, John M. Graham, Kamer Tezcan, G. Bradley Schaefer, Noelle R. Danylchuk, Alexander Asamoah, Kelly E. Jackson, Naomi Yachelevich, Margaret Au, Luis A. Pérez‐Jurado, Tjitske Kleefstra, Peter Penzes
Հրապարակվել է 2019Artigo
Որոնման գործիքներ:
Առնչվող խորագիր
Biology
Gene
Genetics
Missense mutation
Mutation
Phenotype
Cancer research
Cardiology
Cardiomyopathy
Compound heterozygosity
Cyclin-dependent kinase 2
Frameshift mutation
Germline
Germline mutation
Global developmental delay
Haploinsufficiency
Heart failure
Integrin-linked kinase
Intellectual disability
Internal medicine
Kinase
Loss function
Medicine
Neurodevelopmental disorder
Neuroscience
Protein kinase A