PubMed for id: 440897

Year	Number of Results
2006	1
2008	2
2010	1
2011	1
2014	1
2015	2
2016	1
2017	1
2018	2
2019	1
2020	3
2023	1
2024	0

1

3q29 microduplication syndrome: Clinical and molecular description of eleven new cases.

Coyan AG, Dyer LM. Coyan AG, et al. Eur J Med Genet. 2020 Dec;63(12):104083. doi: 10.1016/j.ejmg.2020.104083. Epub 2020 Oct 9. Eur J Med Genet. 2020. PMID: 33039685 Review.

2

Phenotype Heterogeneity in 3q29 Microduplication Syndrome.

Streata I, Riza AL, Sosoi S, Burada F, Ioana M. Streata I, et al. Curr Health Sci J. 2020 Apr-Jun;46(2):193-197. doi: 10.12865/CHSJ.46.02.14. Epub 2020 Jun 30. Curr Health Sci J. 2020. PMID: 32874693 Free PMC article.

3

An Unusual Psychiatric Presentation of the 3q29 Microduplication Syndrome.

Reis F, Pereira C, Laureano M, Cartaxo T. Reis F, et al. Cureus. 2020 Mar 8;12(3):e7203. doi: 10.7759/cureus.7203. Cureus. 2020. PMID: 32269882 Free PMC article.

4

A Case With 4 de Novo Copy Number Variations With Clinical Features That Overlap 1q43q44 Microdeletion and 3q29 Microduplication Syndromes.

Kessi M, Peng J, Yang L, Duan H, Tang Y, Yin F. Kessi M, et al. Child Neurol Open. 2018 Sep 24;5:2329048X18798200. doi: 10.1177/2329048X18798200. eCollection 2018. Child Neurol Open. 2018. PMID: 30263904 Free PMC article.

5

3q29 microduplication syndrome: Description of two new cases and delineation of the minimal critical region.

Tassano E, Uccella S, Giacomini T, Severino M, Siri L, Gherzi M, Celle ME, Porta S, Gimelli G, Ronchetto P. Tassano E, et al. Eur J Med Genet. 2018 Aug;61(8):428-433. doi: 10.1016/j.ejmg.2018.02.011. Epub 2018 Mar 1. Eur J Med Genet. 2018. PMID: 29501613

6

Cerebral palsy, epilepsy, and severe intellectual disability in a patient with 3q29 microduplication syndrome.

Fernández-Jaén A, Castellanos Mdel C, Fernández-Perrone AL, Fernández-Mayoralas DM, de la Vega AG, Calleja-Pérez B, Fernández EC, Albert J, Hombre MC. Fernández-Jaén A, et al. Am J Med Genet A. 2014 Aug;164A(8):2043-7. doi: 10.1002/ajmg.a.36559. Epub 2014 May 16. Am J Med Genet A. 2014. PMID: 24838842

7

[3q29 microduplication syndrome].

Aleixandre Blanquer F, Manchón Trives I, Forniés Arnau MJ, Alcaraz Mas LA, Picó Alfonso N, Galán Sánchez F. Aleixandre Blanquer F, et al. An Pediatr (Barc). 2011 Dec;75(6):409-12. doi: 10.1016/j.anpedi.2011.08.002. Epub 2011 Oct 5. An Pediatr (Barc). 2011. PMID: 21982553 Free article. Spanish.

8

Siblings with phenotypic overlap with Toriello-Carey syndrome and complex cytogenetic imbalances including 3q29 microduplication and 6p25 microdeletion: Review of the literature and additional evidence for genetic heterogeneity.

McGoey R, Varma A, Lacassie Y. McGoey R, et al. Am J Med Genet A. 2010 Dec;152A(12):3068-73. doi: 10.1002/ajmg.a.33721. Am J Med Genet A. 2010. PMID: 21108391 Review.

9

Entire FGF12 duplication by complex chromosomal rearrangements associated with West syndrome.

Oda Y, Uchiyama Y, Motomura A, Fujita A, Azuma Y, Harita Y, Mizuguchi T, Yanagi K, Ogata H, Hata K, Kaname T, Matsubara Y, Wakui K, Matsumoto N. Oda Y, et al. J Hum Genet. 2019 Oct;64(10):1005-1014. doi: 10.1038/s10038-019-0641-1. Epub 2019 Jul 16. J Hum Genet. 2019. PMID: 31311986

10

[Molecular characterisation and phenotypic description of two patients with reciprocal chromosomal aberrations in the region of the 3q29 microdeletion/microduplication syndromes].

Quintela I, Barros-Angueira F, Perez-Gay L, Dacruz D, Castro-Gago M, Carracedo A, Eiris-Punal J. Quintela I, et al. Rev Neurol. 2015 Sep 16;61(6):255-60. Rev Neurol. 2015. PMID: 26350776 Free article. Spanish.

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