Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2016 | 1 |
2018 | 1 |
2019 | 2 |
2024 | 0 |
Search Results
4 results
Results by year
Filters applied: . Clear all
Page 1
Did you mean
daisuke miyauchi
(1 results)?
Retinal structure in Leber's congenital amaurosis caused by RPGRIP1 mutations.
Hum Genome Var. 2019 Jun 27;6:32. doi: 10.1038/s41439-019-0064-8. eCollection 2019.
Hum Genome Var. 2019.
PMID: 31666973
Free PMC article.
X-linked Retinitis Pigmentosa in Japan: Clinical and Genetic Findings in Male Patients and Female Carriers.
Kurata K, Hosono K, Hayashi T, Mizobuchi K, Katagiri S, Miyamichi D, Nishina S, Sato M, Azuma N, Nakano T, Hotta Y.
Kurata K, et al. Among authors: miyamichi d.
Int J Mol Sci. 2019 Mar 26;20(6):1518. doi: 10.3390/ijms20061518.
Int J Mol Sci. 2019.
PMID: 30917587
Free PMC article.
Item in Clipboard
Molecular Diagnosis of 34 Japanese Families with Leber Congenital Amaurosis Using Targeted Next Generation Sequencing.
Hosono K, Nishina S, Yokoi T, Katagiri S, Saitsu H, Kurata K, Miyamichi D, Hikoya A, Mizobuchi K, Nakano T, Minoshima S, Fukami M, Kondo H, Sato M, Hayashi T, Azuma N, Hotta Y.
Hosono K, et al. Among authors: miyamichi d.
Sci Rep. 2018 May 29;8(1):8279. doi: 10.1038/s41598-018-26524-z.
Sci Rep. 2018.
PMID: 29844330
Free PMC article.
Item in Clipboard
Novel HPS6 mutations identified by whole-exome sequencing in two Japanese sisters with suspected ocular albinism.
Miyamichi D, Asahina M, Nakajima J, Sato M, Hosono K, Nomura T, Negishi T, Miyake N, Hotta Y, Ogata T, Matsumoto N.
Miyamichi D, et al.
J Hum Genet. 2016 Sep;61(9):839-42. doi: 10.1038/jhg.2016.56. Epub 2016 May 26.
J Hum Genet. 2016.
PMID: 27225848
Item in Clipboard
Cite
Cite