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
Search Results
2 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
A Nonsense ALMS1 Mutation Underlies Alström Syndrome in an Extended Mennonite Kindred Settled in North Mexico.
Genet Test Mol Biomarkers. 2017 Jun;21(6):397-401. doi: 10.1089/gtmb.2016.0391. Epub 2017 Apr 12.
Genet Test Mol Biomarkers. 2017.
PMID: 28402684
A new missense variant in RAB3GAP2 in a family with muscular dystrophy-short stature and defective autophagy: An expansion of the micro/Martsolf spectrum or a new phenotype?
Mora-Roldan GA, Galaviz-Hernandez C, Hiebert-Froese J, Hernandez A, Montes L, Duran-Pasten ML, Gazarian K, Zenteno JC.
Mora-Roldan GA, et al. Among authors: hiebert froese j.
Am J Med Genet A. 2022 Jul;188(7):1972-1978. doi: 10.1002/ajmg.a.62723. Epub 2022 Mar 11.
Am J Med Genet A. 2022.
PMID: 35274444
Item in Clipboard
Cite
Cite