Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Chinelo Emeka-Nwonovo"'
Autor:
Ellery Santos, Chinelo Emeka‐Nwonovo, Jun Yi Wang, Andrea Schneider, Flora Tassone, Paul Hagerman, Randi Hagerman
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 2, Pp n/a-n/a (2020)
Abstract Background Fragile X mental retardation 1 (FMR1) premutation can cause developmental problems including autism spectrum disorder (ASD), social anxiety, depression, and attention deficit hyperactivity disorder (ADHD). These problems fall unde
Externí odkaz:
https://doaj.org/article/b78ba683a37f4c8e8d99698b7f0d320f
Autor:
Jun Yi Wang, Andrea Schneider, Ellery Santos, Chinelo Emeka-Nwonovo, Randi J Hagerman, Paul J. Hagerman, Flora Tassone
Publikováno v:
Molecular genetics & genomic medicine, vol 8, iss 2
Molecular Genetics & Genomic Medicine, Vol 8, Iss 2, Pp n/a-n/a (2020)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 8, Iss 2, Pp n/a-n/a (2020)
Molecular Genetics & Genomic Medicine
Background Fragile X mental retardation 1 (FMR1) premutation can cause developmental problems including autism spectrum disorder (ASD), social anxiety, depression, and attention deficit hyperactivity disorder (ADHD). These problems fall under an umbr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97200041b3d480a6645d5cb97389c790
https://escholarship.org/uc/item/60r0v4qr
https://escholarship.org/uc/item/60r0v4qr
Autor:
Santos, Ellery1,2 (AUTHOR), Emeka‐Nwonovo, Chinelo1 (AUTHOR), Wang, Jun Yi1,3,4 (AUTHOR), Schneider, Andrea1,2 (AUTHOR), Tassone, Flora1,4 (AUTHOR), Hagerman, Paul1,4 (AUTHOR), Hagerman, Randi1,2 (AUTHOR) rjhagerman@ucdavis.edu
Publikováno v:
Molecular Genetics & Genomic Medicine. Feb2020, Vol. 8 Issue 2, pN.PAG-N.PAG. 1p.