Similar articles for PMID: 25356259

Year	Number of Results
1983	1
1984	1
1990	2
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1996	2
1997	1
1998	3
1999	4
2000	5
2001	5
2003	4
2004	3
2005	1
2006	2
2007	3
2008	4
2009	1
2010	5
2011	4
2012	5
2013	5
2014	2
2015	6
2016	6
2017	5
2018	8
2019	6
2020	2
2021	0

1

Birth of a boy with isolated short stature after prenatal diagnosis of a Xp22.3 nullosomy due to an inherited t(X;15) (p22.3;p10) translocation.

Blondeel E, Molina-Gomes D, Bouhanna P, Fauvert D, Crosnier H, Dessuant H, Vialard F. Blondeel E, et al. Clin Case Rep. 2014 Jun;2(3):98-102. doi: 10.1002/ccr3.71. Epub 2014 May 5. Clin Case Rep. 2014. PMID: 25356259 Free PMC article.

2

Molecular cytogenetic characterization of Xp22.32→pter deletion and Xq26.3→qter duplication in a male fetus associated with 46,Y,rec(X)dup(Xq) inv(X)(p22.3q26.3), a hypoplastic left heart, short stature, and maternal X chromosome pericentric inversion.

Chen CP, Chen CY, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Town DD, Lee MS, Yang CW, Wang W. Chen CP, et al. Taiwan J Obstet Gynecol. 2016 Oct;55(5):705-711. doi: 10.1016/j.tjog.2016.05.009. Taiwan J Obstet Gynecol. 2016. PMID: 27751420 Free article.

3

Short stature in a mother and daughter caused by familial der(X)t(X;X)(p22.1-3;q26).

Reinehr T, Jauch A, Zoll B, Engel U, Bartels I, Andler W. Reinehr T, et al. Am J Med Genet. 2001 Jul 22;102(1):81-5. doi: 10.1002/1096-8628(20010722)102:1<81::aid-ajmg1375>3.0.co;2-v. Am J Med Genet. 2001. PMID: 11471178

4

Genetic counselling in carriers of reciprocal chromosomal translocations involving short arm of chromosome X.

Panasiuk B, Usinskiené R, Kostyk E, Rybałko A, Stasiewicz-Jarocka B, Krzykwa B, Pieńkowska-Grela B, Kucinskas V, Michalova K, Midro AT. Panasiuk B, et al. Ann Genet. 2004 Jan-Mar;47(1):11-28. doi: 10.1016/j.anngen.2004.01.001. Ann Genet. 2004. PMID: 15050871

5

Rare congenital chromosomal aberration dic(X;Y)(p22.33;p11.32) in a patient with primary myelofibrosis.

Pavlistova L, Izakova S, Zemanova Z, Bartuskova L, Langova M, Malikova P, Michalova K. Pavlistova L, et al. Mol Cytogenet. 2016 Aug 31;9(1):67. doi: 10.1186/s13039-016-0276-2. eCollection 2016. Mol Cytogenet. 2016. PMID: 27588041 Free PMC article.

6

Microphthalmia with linear skin defects (MLS) syndrome evaluated by prenatal karyotyping, FISH and array comparative genomic hybridization.

Cain CC, Saul D, Attanasio L, Oehler E, Hamosh A, Blakemore K, Stetten G. Cain CC, et al. Prenat Diagn. 2007 Apr;27(4):373-9. doi: 10.1002/pd.1674. Prenat Diagn. 2007. PMID: 17286317

7

Familial X/Y Translocation Encompassing ARSE in Two Moroccan Siblings with Sensorineural Deafness.

Amasdl S, Smaili W, Natiq A, Hassani A, Sbiti A, Agadr A, Sanlaville D, Sefiani A. Amasdl S, et al. Cytogenet Genome Res. 2017;153(2):66-72. doi: 10.1159/000485071. Epub 2017 Dec 16. Cytogenet Genome Res. 2017. PMID: 29248929

8

Rare inheritance of Leri-Weill Syndrome due to crossover of short stature Homeobox Gene (SHOX) Deletions between X and Y Chromosomes: a case report.

Censani M, Anyane-Yeboa K, Wapner R, Spiegel E, Guzman E, Oberfield SE. Censani M, et al. Int J Pediatr Endocrinol. 2013;2013(1):11. doi: 10.1186/1687-9856-2013-11. Epub 2013 Jun 28. Int J Pediatr Endocrinol. 2013. PMID: 23809065 Free PMC article.

9

[Genetic analysis and prenatal diagnosis for a pregnant woman with an unbalanced t(1;2), t(6;7) translocation and intellectual disability].

Zhang Y, Yang B, Tang X, Chen S, Yu R, He J, Su J, Zhu S, Zhu B. Zhang Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Aug 10;34(4):583-587. doi: 10.3760/cma.j.issn.1003-9406.2017.04.025. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28777864 Chinese.

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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