Similar articles for PMID: 19668335

Year	Number of Results
1993	1
1996	1
1999	1
2003	3
2004	1
2005	4
2006	3
2007	3
2008	3
2009	13
2010	12
2011	8
2012	11
2013	15
2014	10
2015	11
2016	8
2017	6
2018	4
2019	7
2020	3
2021	8
2022	9
2023	3
2024	0

1

Small deletions of SATB2 cause some of the clinical features of the 2q33.1 microdeletion syndrome.

Rosenfeld JA, Ballif BC, Lucas A, Spence EJ, Powell C, Aylsworth AS, Torchia BA, Shaffer LG. Rosenfeld JA, et al. PLoS One. 2009 Aug 10;4(8):e6568. doi: 10.1371/journal.pone.0006568. PLoS One. 2009. PMID: 19668335 Free PMC article.

2

Case series: 2q33.1 microdeletion syndrome--further delineation of the phenotype.

Balasubramanian M, Smith K, Basel-Vanagaite L, Feingold MF, Brock P, Gowans GC, Vasudevan PC, Cresswell L, Taylor EJ, Harris CJ, Friedman N, Moran R, Feret H, Zackai EH, Theisen A, Rosenfeld JA, Parker MJ. Balasubramanian M, et al. J Med Genet. 2011 May;48(5):290-8. doi: 10.1136/jmg.2010.084491. Epub 2011 Feb 22. J Med Genet. 2011. PMID: 21343628 Free article.

3

Specific behavioural phenotype and secondary cognitive decline as a result of an 8.6 Mb deletion of 2q32.2q33.1.

Gregoric Kumperscak H, Krgovic D, Vokac NK. Gregoric Kumperscak H, et al. J Int Med Res. 2016 Apr;44(2):395-402. doi: 10.1177/0300060515595651. Epub 2016 Jan 25. J Int Med Res. 2016. PMID: 26811410 Free PMC article.

4

SATB2-associated syndrome: Mechanisms, phenotype, and practical recommendations.

Zarate YA, Fish JL. Zarate YA, et al. Am J Med Genet A. 2017 Feb;173(2):327-337. doi: 10.1002/ajmg.a.38022. Epub 2016 Oct 24. Am J Med Genet A. 2017. PMID: 27774744 Free PMC article. Review.

5

Further supporting evidence for the SATB2-associated syndrome found through whole exome sequencing.

Zarate YA, Perry H, Ben-Omran T, Sellars EA, Stein Q, Almureikhi M, Simmons K, Klein O, Fish J, Feingold M, Douglas J, Kruer MC, Si Y, Mao R, McKnight D, Gibellini F, Retterer K, Slavotinek A. Zarate YA, et al. Am J Med Genet A. 2015 May;167A(5):1026-32. doi: 10.1002/ajmg.a.36849. Am J Med Genet A. 2015. PMID: 25885067

6

[Analysis of SATB2 gene mutation in a child with Glass syndrome].

Lin M, Yao R, Lu J, Chen W, Xu Y, Li G, Yu T, Qing Y, Jin X, Wang J. Lin M, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jul 10;36(7):712-715. doi: 10.3760/cma.j.issn.1003-9406.2019.07.014. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31302918 Chinese.

7

Intragenic duplication--a novel causative mechanism for SATB2-associated syndrome.

Liedén A, Kvarnung M, Nilssson D, Sahlin E, Lundberg ES. Liedén A, et al. Am J Med Genet A. 2014 Dec;164A(12):3083-7. doi: 10.1002/ajmg.a.36769. Epub 2014 Sep 23. Am J Med Genet A. 2014. PMID: 25251319

8

[Phenotypic and genetic analysis of a sibpair with partial deletion of SATB2 gene caused by 2q33.1 microdeletion].

Jin C, Lei Y, Liu J, Shan Q, Qian B, Zheng F, Chen P, Bai J. Jin C, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jun 10;36(6):628-631. doi: 10.3760/cma.j.issn.1003-9406.2019.06.025. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31055823 Chinese.

9

SATB2-associated syndrome in patients from Japan: Linguistic profiles.

Yamada M, Uehara T, Suzuki H, Takenouchi T, Yoshihashi H, Suzumura H, Mizuno S, Kosaki K. Yamada M, et al. Am J Med Genet A. 2019 Jun;179(6):896-899. doi: 10.1002/ajmg.a.61114. Epub 2019 Mar 7. Am J Med Genet A. 2019. PMID: 30848049

10

Deletion of 4.4 Mb at 2q33.2q33.3 May Cause Growth Deficiency in a Patient with Mental Retardation, Facial Dysmorphic Features and Speech Delay.

Papoulidis I, Paspaliaris V, Papageorgiou E, Siomou E, Dagklis T, Sotiriou S, Thomaidis L, Manolakos E. Papoulidis I, et al. Cytogenet Genome Res. 2015;145(1):19-24. doi: 10.1159/000381568. Epub 2015 Apr 24. Cytogenet Genome Res. 2015. PMID: 25925190

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