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Ken Inoue

Showing results (481-490 of 486) with videos related to

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Aging & Mental Health|December 11, 2019
A systematic review of older adults' request for or attitude toward euthanasia or assisted-suicideDolores Angela Castelli Dransart, Sylvie Lapierre, Annette Erlangsen, et al.
Acta Neuropathologica Communications|December 1, 2020
Down syndrome cell adhesion molecule like-1 (DSCAML1) links the GABA system and seizure susceptibilityYoneko Hayase, Shigeru Amano, Koichi Hashizume, et al.
Plos Genetics|August 5, 2011
Genome-wide association study identifies HLA-DP as a susceptibility gene for pediatric asthma in Asian populationsEmiko Noguchi, Hiromi Sakamoto, Tomomitsu Hirota, et al.
Human Mutation|August 27, 2019
Xq22 deletions and correlation with distinct neurological disease traits in females: Further evidence for a contiguous gene syndromeHadia Hijazi, Fernanda S Coelho, Claudia Gonzaga-Jauregui, et al.
European Journal of Human Genetics : EJHG|March 27, 2023
Molecular diagnosis of 405 individuals with autism spectrum disorderNoriko Miyake, Yoshinori Tsurusaki, Ryoko Fukai, et al.
Journal of Medical Genetics|March 8, 2019
Genetic landscape of Rett syndrome-like phenotypes revealed by whole exome sequencingKazuhiro Iwama, Takeshi Mizuguchi, Eri Takeshita, et al.
Pageof 49

Showing results (481-490 of 486) with videos related to

Sort By:
Pageof 49
You have reached the last page of results.This site can display upto 486 results.
Aging & Mental Health|December 11, 2019
A systematic review of older adults' request for or attitude toward euthanasia or assisted-suicideDolores Angela Castelli Dransart, Sylvie Lapierre, Annette Erlangsen, et al.
Acta Neuropathologica Communications|December 1, 2020
Down syndrome cell adhesion molecule like-1 (DSCAML1) links the GABA system and seizure susceptibilityYoneko Hayase, Shigeru Amano, Koichi Hashizume, et al.
Plos Genetics|August 5, 2011
Genome-wide association study identifies HLA-DP as a susceptibility gene for pediatric asthma in Asian populationsEmiko Noguchi, Hiromi Sakamoto, Tomomitsu Hirota, et al.
Human Mutation|August 27, 2019
Xq22 deletions and correlation with distinct neurological disease traits in females: Further evidence for a contiguous gene syndromeHadia Hijazi, Fernanda S Coelho, Claudia Gonzaga-Jauregui, et al.
European Journal of Human Genetics : EJHG|March 27, 2023
Molecular diagnosis of 405 individuals with autism spectrum disorderNoriko Miyake, Yoshinori Tsurusaki, Ryoko Fukai, et al.
Journal of Medical Genetics|March 8, 2019
Genetic landscape of Rett syndrome-like phenotypes revealed by whole exome sequencingKazuhiro Iwama, Takeshi Mizuguchi, Eri Takeshita, et al.
Pageof 49