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

Year Number of Results
1980 1
1987 1
1998 1
2003 1
2004 1
2007 3
2008 1
2011 1
2012 2
2013 1
2014 3
2017 1
2018 2
2019 2
2020 2
2022 2
2023 1
2024 0

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PubMed for id: 1842509

23 results

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Page 1
Multiparameter Investigation of a 46,XX/46,XY Tetragametic Chimeric Phenotypical Male Patient with Bilateral Scrotal Ovotestes and Ovulatory Activity.
van Bever Y, Wolffenbuttel KP, Brüggenwirth HT, Blom E, de Klein A, Eussen BHJ, van der Windt F, Hannema SE, Dessens AB, Dorssers LCJ, Biermann K, Hersmus R, de Rijke YB, Looijenga LHJ. van Bever Y, et al. Sex Dev. 2018;12(1-3):145-154. doi: 10.1159/000479946. Epub 2017 Sep 20. Sex Dev. 2018. PMID: 28926831 Free PMC article.
Mutations in FEZF1 cause Kallmann syndrome.
Kotan LD, Hutchins BI, Ozkan Y, Demirel F, Stoner H, Cheng PJ, Esen I, Gurbuz F, Bicakci YK, Mengen E, Yuksel B, Wray S, Topaloglu AK. Kotan LD, et al. Am J Hum Genet. 2014 Sep 4;95(3):326-31. doi: 10.1016/j.ajhg.2014.08.006. Am J Hum Genet. 2014. PMID: 25192046 Free PMC article.
23 results