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 |
---|---|
2018 | 2 |
2019 | 3 |
2024 | 0 |
Search Results
5 results
Results by year
Filters applied: . Clear all
Page 1
Distinctive epigenomes characterize glioma stem cells and their response to differentiation cues.
Genome Biol. 2018 Mar 27;19(1):43. doi: 10.1186/s13059-018-1420-6.
Genome Biol. 2018.
PMID: 29587824
Free PMC article.
Familial chronic megacolon presenting in childhood or adulthood: Seeking the presumed gene association.
Camilleri M, Wieben E, Eckert D, Carlson P, Hurley O'Dwyer R, Gibbons D, Acosta A, Klee EW.
Camilleri M, et al.
Neurogastroenterol Motil. 2019 Apr;31(4):e13550. doi: 10.1111/nmo.13550. Epub 2019 Jan 20.
Neurogastroenterol Motil. 2019.
PMID: 30663199
Free PMC article.
Item in Clipboard
Molecular characterization of known and novel ACVR1 variants in phenotypes of aberrant ossification.
Gupta A, Zimmermann MT, Wang H, Broski SM, Sigafoos AN, Macklin SK, Urrutia RA, Clark KJ, Atwal PS, Pignolo RJ, Klee EW.
Gupta A, et al.
Am J Med Genet A. 2019 Sep;179(9):1764-1777. doi: 10.1002/ajmg.a.61274. Epub 2019 Jun 26.
Am J Med Genet A. 2019.
PMID: 31240838
Item in Clipboard
A case of YY1-associated syndromic learning disability or Gabriele-de Vries syndrome with myasthenia gravis.
Morales-Rosado JA, Kaiwar C, Smith BE, Klee EW, Dhamija R.
Morales-Rosado JA, et al.
Am J Med Genet A. 2018 Dec;176(12):2846-2849. doi: 10.1002/ajmg.a.40626. Epub 2018 Dec 14.
Am J Med Genet A. 2018.
PMID: 30549423
Item in Clipboard
De novo DDX3X missense variants in males appear viable and contribute to syndromic intellectual disability.
Nicola P, Blackburn PR, Rasmussen KJ, Bertsch NL, Klee EW, Hasadsri L, Pichurin PN, Rankin J, Raymond FL; DDD Study; Clayton-Smith J.
Nicola P, et al.
Am J Med Genet A. 2019 Apr;179(4):570-578. doi: 10.1002/ajmg.a.61061. Epub 2019 Feb 7.
Am J Med Genet A. 2019.
PMID: 30734472
Item in Clipboard
Cite
Cite