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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2011 | 1 |
2012 | 1 |
2013 | 1 |
2014 | 2 |
2015 | 2 |
2024 | 0 |
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Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome.
G3 (Bethesda). 2015 Sep 16;5(11):2453-61. doi: 10.1534/g3.115.021345.
G3 (Bethesda). 2015.
PMID: 26384369
Free PMC article.
Reproductive Health Issues for Adults with a Common Genomic Disorder: 22q11.2 Deletion Syndrome.
Chan C, Costain G, Ogura L, Silversides CK, Chow EW, Bassett AS.
Chan C, et al.
J Genet Couns. 2015 Oct;24(5):810-21. doi: 10.1007/s10897-014-9811-7. Epub 2015 Jan 13.
J Genet Couns. 2015.
PMID: 25579115
Free PMC article.
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Prevalence of hypocalcaemia and its associated features in 22q11·2 deletion syndrome.
Cheung EN, George SR, Costain GA, Andrade DM, Chow EW, Silversides CK, Bassett AS.
Cheung EN, et al.
Clin Endocrinol (Oxf). 2014 Aug;81(2):190-6. doi: 10.1111/cen.12466. Epub 2014 May 27.
Clin Endocrinol (Oxf). 2014.
PMID: 24735350
Free PMC article.
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Reproductive fitness and genetic transmission of tetralogy of Fallot in the molecular age.
Chin-Yee NJ, Costain G, Swaby JA, Silversides CK, Bassett AS.
Chin-Yee NJ, et al.
Circ Cardiovasc Genet. 2014 Apr;7(2):102-9. doi: 10.1161/CIRCGENETICS.113.000328. Epub 2014 Feb 21.
Circ Cardiovasc Genet. 2014.
PMID: 24563425
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Premorbid adjustment and schizophrenia in individuals with 22q11.2 deletion syndrome.
Yuen T, Chow EW, Silversides CK, Bassett AS.
Yuen T, et al.
Schizophr Res. 2013 Dec;151(1-3):221-5. doi: 10.1016/j.schres.2013.10.041. Epub 2013 Nov 19.
Schizophr Res. 2013.
PMID: 24262682
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Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathways.
Silversides CK, Lionel AC, Costain G, Merico D, Migita O, Liu B, Yuen T, Rickaby J, Thiruvahindrapuram B, Marshall CR, Scherer SW, Bassett AS.
Silversides CK, et al.
PLoS Genet. 2012;8(8):e1002843. doi: 10.1371/journal.pgen.1002843. Epub 2012 Aug 9.
PLoS Genet. 2012.
PMID: 22912587
Free PMC article.
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Sex differences in reproductive fitness contribute to preferential maternal transmission of 22q11.2 deletions.
Costain G, Chow EW, Silversides CK, Bassett AS.
Costain G, et al.
J Med Genet. 2011 Dec;48(12):819-24. doi: 10.1136/jmedgenet-2011-100440. Epub 2011 Nov 2.
J Med Genet. 2011.
PMID: 22051516
Free article.
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