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
5 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Identifying candidate genes for 2p15p16.1 microdeletion syndrome using clinical, genomic, and functional analysis.
JCI Insight. 2016 Mar 17;1(3):e85461. doi: 10.1172/jci.insight.85461.
JCI Insight. 2016.
PMID: 27699255
Free PMC article.
Exome sequencing identified a de novo mutation of PURA gene in a patient with familial Xp22.31 microduplication.
Qiao Y, Bagheri H, Tang F, Badduke C, Martell S, Lewis SME, Robinson W, Connolly MB, Arbour L, Rajcan-Separovic E.
Qiao Y, et al. Among authors: badduke c.
Eur J Med Genet. 2019 Feb;62(2):103-108. doi: 10.1016/j.ejmg.2018.06.010. Epub 2018 Jun 13.
Eur J Med Genet. 2019.
PMID: 29908350
Item in Clipboard
miRNA and miRNA target genes in copy number variations occurring in individuals with intellectual disability.
Qiao Y, Badduke C, Mercier E, Lewis SM, Pavlidis P, Rajcan-Separovic E.
Qiao Y, et al. Among authors: badduke c.
BMC Genomics. 2013 Aug 10;14:544. doi: 10.1186/1471-2164-14-544.
BMC Genomics. 2013.
PMID: 23937676
Free PMC article.
Item in Clipboard
Whole exome sequencing of families with 1q21.1 microdeletion or microduplication.
Qiao Y, Badduke C, Tang F, Cowieson D, Martell S, Lewis SME, Peñaherrera MS, Robinson WP, Volchuk A, Rajcan-Separovic E.
Qiao Y, et al. Among authors: badduke c.
Am J Med Genet A. 2017 Jul;173(7):1782-1791. doi: 10.1002/ajmg.a.38247. Epub 2017 May 5.
Am J Med Genet A. 2017.
PMID: 28475290
Item in Clipboard
Comprehensive characterization of a Canadian cohort of von Hippel-Lindau disease patients.
Salama Y, Albanyan S, Szybowska M, Bullivant G, Gallinger B, Giles RH, Asa S, Badduke C, Chiorean A, Druker H, Ezzat S, Hannah-Shmouni F, Hernandez KG, Inglese C, Jani P, Kaur Y, Krema H, Krimus L, Laperriere N, Lichner Z, Mete O, Sit M, Zadeh G, Jewett MAS, Malkin D, Stockley T, Wasserman JD, Xu W, Schachter NF, Kim RH.
Salama Y, et al. Among authors: badduke c.
Clin Genet. 2019 Nov;96(5):461-467. doi: 10.1111/cge.13613. Epub 2019 Aug 6.
Clin Genet. 2019.
PMID: 31368132
Item in Clipboard
Cite
Cite