Similar articles for PMID: 21088380

Year	Number of Results
1991	1
1992	1
1993	1
1994	1
1995	2
1996	1
1997	3
2000	1
2001	2
2002	6
2003	8
2004	5
2005	8
2006	16
2007	10
2008	17
2009	10
2010	14
2011	10
2012	16
2013	17
2014	10
2015	7
2016	8
2017	5
2018	7
2019	6
2020	3
2021	2
2022	3
2024	0

1

Identification of new susceptibility regions for X;Y translocations in patients with testicular disorder of sex development.

Beaulieu Bergeron M, Lemyre E, Lemieux N. Beaulieu Bergeron M, et al. Sex Dev. 2011;5(1):1-6. doi: 10.1159/000321995. Epub 2010 Nov 17. Sex Dev. 2011. PMID: 21088380

2

Two males with SRY-positive 46,XX testicular disorder of sex development.

Gunes S, Asci R, Okten G, Atac F, Onat OE, Ogur G, Aydin O, Ozcelik T, Bagci H. Gunes S, et al. Syst Biol Reprod Med. 2013 Feb;59(1):42-7. doi: 10.3109/19396368.2012.731624. Epub 2012 Oct 30. Syst Biol Reprod Med. 2013. PMID: 23110663

3

[Molecular and cytogenetic characterization of six 46, XX males due to translocations between the short arms of X and Y chromosomes].

Xing Y, Ji X, Xiao B, Jiang WT, Hu Q, Hu J, Cao Y, Tao J. Xing Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Aug;29(4):408-12. doi: 10.3760/cma.j.issn.1003-9406.2012.04.007. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22875496 Chinese.

4

Clinical and molecular studies in four patients with SRY-positive 46,XX testicular disorders of sex development: implications for variable sex development and genomic rearrangements.

Nakashima S, Ohishi A, Takada F, Kawamura H, Igarashi M, Fukami M, Ogata T. Nakashima S, et al. J Hum Genet. 2014 Oct;59(10):549-53. doi: 10.1038/jhg.2014.70. Epub 2014 Aug 7. J Hum Genet. 2014. PMID: 25102093

5

Abnormal XY interchange between a novel isolated protein kinase gene, PRKY, and its homologue, PRKX, accounts for one third of all (Y+)XX males and (Y-)XY females.

Schiebel K, Winkelmann M, Mertz A, Xu X, Page DC, Weil D, Petit C, Rappold GA. Schiebel K, et al. Hum Mol Genet. 1997 Oct;6(11):1985-9. doi: 10.1093/hmg/6.11.1985. Hum Mol Genet. 1997. PMID: 9302280

6

Identification and characterization of an Xp22.33;Yp11.2 translocation causing a triplication of several genes of the pseudoautosomal region 1 in an XX male patient with severe systemic lupus erythematosus.

Chagnon P, Schneider R, Hébert J, Fortin PR, Provost S, Belisle C, Gingras M, Bolduc V, Perreault C, Silverman E, Busque L. Chagnon P, et al. Arthritis Rheum. 2006 Apr;54(4):1270-8. doi: 10.1002/art.21733. Arthritis Rheum. 2006. PMID: 16575839 Free article.

7

[Molecular analysis of the Y chromosome in XX sex-reversed patients].

Chernykh VB, Chukhrova AL, Vasserman NN, Il'ina EV, Karmanov ME, Fedotov VP, Poliakov AV. Chernykh VB, et al. Genetika. 2008 Feb;44(2):236-41. Genetika. 2008. PMID: 18619043 Russian.

8

Mixed gonadal dysgenesis with 45,X/46,X,idic(Y)/46,XY,idic(Y) karyotype.

Caglayan AO, Demiryilmaz F, Kendirci M, Ozyazgan I, Akalin H, Bittmann S. Caglayan AO, et al. Genet Couns. 2009;20(2):173-9. Genet Couns. 2009. PMID: 19650415

9

Evidence for high breakpoint variability in 46, XX, SRY-positive testicular disorder and frequent ARSE deletion that may be associated with short stature.

Capron C, Januel L, Vieville G, Jaillard S, Kuentz P, Salaun G, Nadeau G, Clement P, Brechard MP, Herve B, Dupont JM, Gruchy N, Chambon P, Abdelhedi F, Dahlen E, Vago P, Harbuz R, Plotton I, Coutton C, Belaud-Rotureau MA, Schluth-Bolard C, Vialard F. Capron C, et al. Andrology. 2022 Nov;10(8):1625-1631. doi: 10.1111/andr.13279. Epub 2022 Sep 7. Andrology. 2022. PMID: 36026611 Free article.

10

Array-CGH characterization of a prenatally detected de novo 46,X,der(Y)t(X;Y)(p22.3;q11.2) in a male fetus.

Palka C, Alfonsi M, Morizio E, Soranno A, La Rovere D, Matarrelli B, Rullo AL, Zori R, Chiarelli F, Calabrese G. Palka C, et al. Eur J Med Genet. 2011 May-Jun;54(3):333-6. doi: 10.1016/j.ejmg.2011.02.003. Epub 2011 Feb 24. Eur J Med Genet. 2011. PMID: 21354345

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