Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Erin Harward"'
Autor:
Marc Woodbury-Smith, E. Robert Wassman, Nadeem Murtaza, James Stavropoulos, Stephen W. Scherer, Erin Harward, Vickie Kwan, Sylvia Lamoureux, Biren M. Dave, Leon Chalil, Marsha Speevak, Nicholas Holzapfel, Lia D’Abate, Sean H. White, Jacob Nielsen, Mohammed Uddin, Thomas Nalpathamkalam, Brad Doble, Karun K. Singh, John Wei, Kristin J Hope, Giovanna Pellecchia, Brianna K. Unda, Karen S. Ho
Publikováno v:
American Journal of Human Genetics
Copy-number variations (CNVs) are strong risk factors for neurodevelopmental and psychiatric disorders. The 15q13.3 microdeletion syndrome region contains up to ten genes and is associated with numerous conditions, including autism spectrum disorder
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe1b0e101470cca83445b2de71df3227
https://pubmed.ncbi.nlm.nih.gov/29395074
https://pubmed.ncbi.nlm.nih.gov/29395074
Autor:
Moises A. Serrano, Rena Vanzo, Karen S. Ho, Megan M. Martin, Hope Twede, E. Robert Wassman, Patricia Mowery-Rushton, Stephanie Page, Erin Harward, Andreas Peiffer, Charles H. Hensel
Publikováno v:
BioMed Research International, Vol 2016 (2016)
BioMed Research International
BioMed Research International
Copy number variants (CNVs) as detected by chromosomal microarray analysis (CMA) significantly contribute to the etiology of neurodevelopmental disorders, such as developmental delay (DD), intellectual disability (ID), and autism spectrum disorder (A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee2f1cd1548a295f4cd8b2471d1d9d85
https://doaj.org/article/b0ac558de9a24d41883c9f5834edfb7f
https://doaj.org/article/b0ac558de9a24d41883c9f5834edfb7f
Autor:
Davis, Kyle Walter1 (AUTHOR) kdavis@lineagen.com, Hamby Erby, Lori2 (AUTHOR), Fiallos, Katie3 (AUTHOR), Martin, Megan1 (AUTHOR), Wassman, Edward Robert1 (AUTHOR)
Publikováno v:
Molecular Genetics & Genomic Medicine. Jul2019, Vol. 7 Issue 7, pN.PAG-N.PAG. 1p.
Autor:
Rina Kansal
The book is written and edited by an individual fortunate to see and work through the evolution of precision medicine in the last three decades. The book begins with an introduction to genomics and precision medicine, followed by a chapter on pediatr
