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 |
---|---|
2019 | 1 |
2020 | 1 |
2021 | 1 |
2023 | 1 |
2024 | 0 |
Search Results
4 results
Results by year
Filters applied: . Clear all
Page 1
Pioneer factor ASCL1 cooperates with the mSWI/SNF complex at distal regulatory elements to regulate human neural differentiation.
Genes Dev. 2023 Mar 1;37(5-6):218-242. doi: 10.1101/gad.350269.122. Epub 2023 Mar 17.
Genes Dev. 2023.
PMID: 36931659
Free PMC article.
Inflammatory Arthritis as a Possible Feature of Coffin-Siris Syndrome.
Melo Gomes S, Dias C, Omoyinmi E, Compeyrot-Lacassagne S, Klein N, Sebire NJ, Brogan P.
Melo Gomes S, et al.
Pediatrics. 2019 Jul;144(1):e20181741. doi: 10.1542/peds.2018-1741.
Pediatrics. 2019.
PMID: 31243159
Item in Clipboard
Generation of an iPSC line (CRICKi001-A) from an individual with a germline SMARCA4 missense mutation and autism spectrum disorder.
Devito LG, Healy L, Mohammed S, Guillemot F, Dias C.
Devito LG, et al.
Stem Cell Res. 2021 May;53:102304. doi: 10.1016/j.scr.2021.102304. Epub 2021 Mar 20.
Stem Cell Res. 2021.
PMID: 33799280
Free PMC article.
Item in Clipboard
De novo SMARCA2 variants clustered outside the helicase domain cause a new recognizable syndrome with intellectual disability and blepharophimosis distinct from Nicolaides-Baraitser syndrome.
Cappuccio G, Sayou C, Tanno PL, Tisserant E, Bruel AL, Kennani SE, Sá J, Low KJ, Dias C, Havlovicová M, Hančárová M, Eichler EE, Devillard F, Moutton S, Van-Gils J, Dubourg C, Odent S, Gerard B, Piton A, Yamamoto T, Okamoto N, Firth H, Metcalfe K, Moh A, Chapman KA, Aref-Eshghi E, Kerkhof J, Torella A, Nigro V, Perrin L, Piard J, Le Guyader G, Jouan T, Thauvin-Robinet C, Duffourd Y, George-Abraham JK, Buchanan CA, Williams D, Kini U, Wilson K; Telethon Undiagnosed Diseases Program; Sousa SB, Hennekam RCM, Sadikovic B, Thevenon J, Govin J, Vitobello A, Brunetti-Pierri N.
Cappuccio G, et al.
Genet Med. 2020 Nov;22(11):1838-1850. doi: 10.1038/s41436-020-0898-y. Epub 2020 Jul 22.
Genet Med. 2020.
PMID: 32694869
Free article.
Item in Clipboard
Cite
Cite