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

Year Number of Results
1991 2
1995 1
1999 1
2000 1
2005 3
2007 1
2009 1
2010 3
2012 1
2013 1
2014 2
2015 1
2016 1
2017 2
2018 4
2019 1
2024 0

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PubMed (cited) for id: 107773

22 results

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Page 1
The Natural History of a Man With Ovotesticular 46,XX DSD Caused by a Novel 3-Mb 15q26.2 Deletion Containing NR2F2 Gene.
Carvalheira G, Malinverni AM, Moysés-Oliveira M, Ueta R, Cardili L, Monteagudo P, Mathez ALG, Verreschi IT, Maluf MA, Shida MEF, Leite MTC, Mazzotti D, Melaragno MI, Dias-da-Silva MR. Carvalheira G, et al. J Endocr Soc. 2019 Aug 28;3(11):2107-2113. doi: 10.1210/js.2019-00241. eCollection 2019 Nov 1. J Endocr Soc. 2019. PMID: 31687637 Free PMC article.
Single-cell analysis of early progenitor cells that build coronary arteries.
Su T, Stanley G, Sinha R, D'Amato G, Das S, Rhee S, Chang AH, Poduri A, Raftrey B, Dinh TT, Roper WA, Li G, Quinn KE, Caron KM, Wu S, Miquerol L, Butcher EC, Weissman I, Quake S, Red-Horse K. Su T, et al. Nature. 2018 Jul;559(7714):356-362. doi: 10.1038/s41586-018-0288-7. Epub 2018 Jul 4. Nature. 2018. PMID: 29973725 Free PMC article.
Loss of Function of the Nuclear Receptor NR2F2, Encoding COUP-TF2, Causes Testis Development and Cardiac Defects in 46,XX Children.
Bashamboo A, Eozenou C, Jorgensen A, Bignon-Topalovic J, Siffroi JP, Hyon C, Tar A, Nagy P, Sólyom J, Halász Z, Paye-Jaouen A, Lambert S, Rodriguez-Buritica D, Bertalan R, Martinerie L, Rajpert-De Meyts E, Achermann JC, McElreavey K. Bashamboo A, et al. Am J Hum Genet. 2018 Mar 1;102(3):487-493. doi: 10.1016/j.ajhg.2018.01.021. Epub 2018 Feb 22. Am J Hum Genet. 2018. PMID: 29478779 Free PMC article.
Rare variants in NR2F2 cause congenital heart defects in humans.
Al Turki S, Manickaraj AK, Mercer CL, Gerety SS, Hitz MP, Lindsay S, D'Alessandro LC, Swaminathan GJ, Bentham J, Arndt AK, Louw J, Low J, Breckpot J, Gewillig M, Thienpont B, Abdul-Khaliq H, Harnack C, Hoff K, Kramer HH, Schubert S, Siebert R, Toka O, Cosgrove C, Watkins H, Lucassen AM, O'Kelly IM, Salmon AP, Bu'lock FA, Granados-Riveron J, Setchfield K, Thornborough C, Brook JD, Mulder B, Klaassen S, Bhattacharya S, Devriendt K, Fitzpatrick DF; UK10K Consortium; Wilson DI, Mital S, Hurles ME. Al Turki S, et al. Am J Hum Genet. 2014 Apr 3;94(4):574-85. doi: 10.1016/j.ajhg.2014.03.007. Am J Hum Genet. 2014. PMID: 24702954 Free PMC article.
22 results