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

Year Number of Results
1996 1
1998 1
2000 1
2001 1
2007 4
2008 2
2009 1
2010 2
2011 3
2012 4
2013 1
2014 6
2015 9
2016 10
2017 17
2018 7
2019 16
2020 6
2021 6
2022 2
2023 4
2024 0

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Similar articles for PMID: 31687637

92 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.
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.
SRY-negative 46,XX testicular/ovotesticular DSD: Long-term outcomes and early blockade of gonadotropic axis.
Lambert S, Peycelon M, Samara-Boustani D, Hyon C, Dumeige L, Peuchmaur M, Fiot E, Léger J, Simon D, Paye-Jaouen A, Bouligand J, Siffroi JP, Carel JC, McElreavey K, El Ghoneimi A, Brachet C, Bouvattier C, Martinerie L. Lambert S, et al. Clin Endocrinol (Oxf). 2021 Apr;94(4):667-676. doi: 10.1111/cen.14389. Epub 2020 Dec 26. Clin Endocrinol (Oxf). 2021. PMID: 33296530
A 46,XX testicular disorder of sex development caused by a Wilms' tumour Factor-1 (WT1) pathogenic variant.
Gomes NL, de Paula LCP, Silva JM, Silva TE, Lerário AM, Nishi MY, Batista RL, Faria Júnior JAD, Moraes D, Costa EMF, Hemesath TP, Guaragna-Filho G, Leite JCL, Carvalho CG, Domenice S, Costa EC, Mendonca BB. Gomes NL, et al. Clin Genet. 2019 Jan;95(1):172-176. doi: 10.1111/cge.13459. Epub 2018 Oct 28. Clin Genet. 2019. PMID: 30294972 Free article.
92 results