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

Year Number of Results
1949 2
1952 1
1962 1
1971 1
1990 1
1991 1
1994 1
1998 2
2001 1
2002 1
2005 1
2006 1
2007 1
2008 4
2009 4
2010 5
2011 2
2012 10
2013 13
2014 12
2015 7
2016 9
2017 13
2018 11
2019 5
2020 2
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Similar Articles for PMID: 32123124

94 results
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Case 2: GATA6 Mutation Responsible for Multiple Congenital Anomalies in 2 Siblings.
Juneau J, Wright T, Turcu R. Juneau J, et al. Neoreviews. 2020 Mar;21(3):e196-e198. doi: 10.1542/neo.21-3-e196. Neoreviews. 2020. PMID: 32123124 No abstract available.
Case report: maternal mosaicism resulting in inheritance of a novel GATA6 mutation causing pancreatic agenesis and neonatal diabetes mellitus.
Yau D, De Franco E, Flanagan SE, Ellard S, Blumenkrantz M, Mitchell JJ. Yau D, et al. Diagn Pathol. 2017 Jan 3;12(1):1. doi: 10.1186/s13000-016-0592-1. Diagn Pathol. 2017. PMID: 28049534 Free PMC article.
Whole exome sequencing identifies de novo mutations in GATA6 associated with congenital diaphragmatic hernia.
Yu L, Bennett JT, Wynn J, Carvill GL, Cheung YH, Shen Y, Mychaliska GB, Azarow KS, Crombleholme TM, Chung DH, Potoka D, Warner BW, Bucher B, Lim FY, Pietsch J, Stolar C, Aspelund G, Arkovitz MS; University of Washington Center for Mendelian Genomics, Mefford H, Chung WK. Yu L, et al. J Med Genet. 2014 Mar;51(3):197-202. doi: 10.1136/jmedgenet-2013-101989. Epub 2014 Jan 2. J Med Genet. 2014. PMID: 24385578 Free PMC article.
First report of a de novo 18q11.2 microdeletion including GATA6 associated with complex congenital heart disease and renal abnormalities.
Bui PH, Dorrani N, Wong D, Perens G, Dipple KM, Quintero-Rivera F. Bui PH, et al. Am J Med Genet A. 2013 Jul;161A(7):1773-8. doi: 10.1002/ajmg.a.35974. Epub 2013 May 21. Am J Med Genet A. 2013. PMID: 23696469
A case of pancreatic agenesis and congenital heart defects with a novel GATA6 nonsense mutation: evidence of haploinsufficiency due to nonsense-mediated mRNA decay.
Suzuki S, Nakao A, Sarhat AR, Furuya A, Matsuo K, Tanahashi Y, Kajino H, Azuma H. Suzuki S, et al. Am J Med Genet A. 2014 Feb;164A(2):476-9. doi: 10.1002/ajmg.a.36275. Epub 2013 Dec 5. Am J Med Genet A. 2014. PMID: 24310933
GATA6 loss-of-function mutation contributes to congenital bicuspid aortic valve.
Xu YJ, Di RM, Qiao Q, Li XM, Huang RT, Xue S, Liu XY, Wang J, Yang YQ. Xu YJ, et al. Gene. 2018 Jul 15;663:115-120. doi: 10.1016/j.gene.2018.04.018. Epub 2018 Apr 10. Gene. 2018. PMID: 29653232
Congenital Anomalies of the Extremities Occurring in Siblings.
Takagi T, Seki A, Mochida J, Takayama S. Takagi T, et al. J Hand Surg Asian Pac Vol. 2016 Feb;21(1):49-53. doi: 10.1142/S2424835516500065. J Hand Surg Asian Pac Vol. 2016. PMID: 27454502
A novel GATA6 mutation associated with congenital ventricular septal defect.
Zheng GF, Wei D, Zhao H, Zhou N, Yang YQ, Liu XY. Zheng GF, et al. Int J Mol Med. 2012 Jun;29(6):1065-71. doi: 10.3892/ijmm.2012.930. Epub 2012 Mar 7. Int J Mol Med. 2012. PMID: 22407241
A novel GATA6 mutation leading to congenital heart defects and permanent neonatal diabetes: a case report.
Catli G, Abaci A, Flanagan SE, De Franco E, Ellard S, Hattersley A, Guleryuz H, Bober E. Catli G, et al. Diabetes Metab. 2013 Sep;39(4):370-4. doi: 10.1016/j.diabet.2013.01.005. Epub 2013 Apr 30. Diabetes Metab. 2013. PMID: 23639568
A novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect.
Lin X, Huo Z, Liu X, Zhang Y, Li L, Zhao H, Yan B, Liu Y, Yang Y, Chen YH. Lin X, et al. J Hum Genet. 2010 Oct;55(10):662-7. doi: 10.1038/jhg.2010.84. Epub 2010 Jul 15. J Hum Genet. 2010. PMID: 20631719
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