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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2005 2
2006 1
2007 5
2008 8
2009 4
2010 4
2011 5
2012 1
2013 7
2014 6
2015 1
2016 3
2017 3
2018 4
2019 5
2020 3
2021 1
2022 2
2024 0

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58 results

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Page 1
X-chromosome association studies of congenital heart defects.
Agopian AJ, Hoang TT, Goldmuntz E, Hakonarson H, Musfee FI, Mitchell LE; Pediatric Cardiac Genomics Consortium. Agopian AJ, et al. Am J Med Genet A. 2020 Jan;182(1):250-254. doi: 10.1002/ajmg.a.61411. Epub 2019 Nov 15. Am J Med Genet A. 2020. PMID: 31729158 Free PMC article. No abstract available.
The Congenital Heart Disease Genetic Network Study: Cohort description.
Hoang TT, Goldmuntz E, Roberts AE, Chung WK, Kline JK, Deanfield JE, Giardini A, Aleman A, Gelb BD, Mac Neal M, Porter GA Jr, Kim R, Brueckner M, Lifton RP, Edman S, Woyciechowski S, Mitchell LE, Agopian AJ. Hoang TT, et al. PLoS One. 2018 Jan 19;13(1):e0191319. doi: 10.1371/journal.pone.0191319. eCollection 2018. PLoS One. 2018. PMID: 29351346 Free PMC article.
Subtelomeric deletions of chromosome 6p: molecular and cytogenetic characterization of three new cases with phenotypic overlap with Ritscher-Schinzel (3C) syndrome.
Descipio C, Schneider L, Young TL, Wasserman N, Yaeger D, Lu F, Wheeler PG, Williams MS, Bason L, Jukofsky L, Menon A, Geschwindt R, Chudley AE, Saraiva J, Schinzel AA, Guichet A, Dobyns WE, Toutain A, Spinner NB, Krantz ID. Descipio C, et al. Am J Med Genet A. 2005 Apr 1;134A(1):3-11. doi: 10.1002/ajmg.a.30573. Am J Med Genet A. 2005. PMID: 15704124 Review.
58 results