Similar articles for PMID: 24510684

Year	Number of Results
2004	3
2005	1
2006	3
2007	3
2008	3
2009	5
2010	3
2011	11
2012	10
2013	7
2014	9
2015	11
2016	11
2017	9
2018	8
2019	8
2020	4
2021	10
2022	6
2023	5
2024	0

1

Molecular analysis of fragile X syndrome.

Basehore MJ, Friez MJ. Basehore MJ, et al. Curr Protoc Hum Genet. 2014 Jan 21;80:9.5.1-9.5.19. doi: 10.1002/0471142905.hg0905s80. Curr Protoc Hum Genet. 2014. PMID: 24510684

2

Molecular analysis of Fragile X syndrome.

Basehore MJ, Friez MJ. Basehore MJ, et al. Curr Protoc Hum Genet. 2009 Oct;Chapter 9:Unit 9.5. doi: 10.1002/0471142905.hg0905s63. Curr Protoc Hum Genet. 2009. PMID: 19806593

3

Partially methylated alleles, microdeletion, and tissue mosaicism in a fragile X male with tremor and ataxia at 30 years of age: A case report.

Hwang YT, Aliaga SM, Arpone M, Francis D, Li X, Chong B, Slater HR, Rogers C, Bretherton L, Hunter M, Heard R, Godler DE. Hwang YT, et al. Am J Med Genet A. 2016 Dec;170(12):3327-3332. doi: 10.1002/ajmg.a.37954. Epub 2016 Oct 1. Am J Med Genet A. 2016. PMID: 27696642

4

EMQN best practice guidelines for the molecular genetic testing and reporting of fragile X syndrome and other fragile X-associated disorders.

Biancalana V, Glaeser D, McQuaid S, Steinbach P. Biancalana V, et al. Eur J Hum Genet. 2015 Apr;23(4):417-25. doi: 10.1038/ejhg.2014.185. Epub 2014 Sep 17. Eur J Hum Genet. 2015. PMID: 25227148 Free PMC article.

5

Unstable mutations in the FMR1 gene and the phenotypes.

Loesch D, Hagerman R. Loesch D, et al. Adv Exp Med Biol. 2012;769:78-114. doi: 10.1007/978-1-4614-5434-2_6. Adv Exp Med Biol. 2012. PMID: 23560306 Free PMC article. Review.

6

Unraveling unusual X-chromosome patterns during fragile-X syndrome genetic testing.

Esposito G, Tremolaterra MR, Savarese M, Spiniello M, Patrizio MP, Lombardo B, Pastore L, Salvatore F, Carsana A. Esposito G, et al. Clin Chim Acta. 2018 Jan;476:167-172. doi: 10.1016/j.cca.2017.11.016. Epub 2017 Nov 21. Clin Chim Acta. 2018. PMID: 29170104 Free article.

7

[FMR1 PREMUTATION CARRIERS - ARE THEY REALLY ASYMPTOMATIC?].

Elizur S, Berkenstadt M, Ries-Levavi L, Gruber N, Pinhas-Hamiel O, Hassin-Baer S, Raas-Rothschild A, Raanani H, Cukierman-Yaffe T, Orvieto R, Cohen Y, Gabis L. Elizur S, et al. Harefuah. 2018 Apr;157(4):241-244. Harefuah. 2018. PMID: 29688643 Review. Hebrew.

8

[Triplet expansion cytosine-guanine-guanine: Three cases of OMIM syndrome in the same family].

González-Pérez J, Izquierdo-Álvarez S, Fuertes-Rodrigo C, Monge-Galindo L, Peña-Segura JL, López-Pisón FJ. González-Pérez J, et al. Med Clin (Barc). 2016 Apr 1;146(7):311-5. doi: 10.1016/j.medcli.2015.11.022. Epub 2016 Jan 6. Med Clin (Barc). 2016. PMID: 26776484 Spanish.

9

Characterization and Early Detection of Balance Deficits in Fragile X Premutation Carriers With and Without Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS).

O'Keefe JA, Robertson-Dick E, Dunn EJ, Li Y, Deng Y, Fiutko AN, Berry-Kravis E, Hall DA. O'Keefe JA, et al. Cerebellum. 2015 Dec;14(6):650-62. doi: 10.1007/s12311-015-0659-7. Cerebellum. 2015. PMID: 25763861

10

Fragile X syndrome full mutation in cognitively normal male identified as part of an Australian reproductive carrier screening program.

Jarmolowicz AI, Baker EK, Bartlett E, Francis D, Ling L, Gamage D, Delatycki MB, Godler DE. Jarmolowicz AI, et al. Am J Med Genet A. 2021 May;185(5):1498-1503. doi: 10.1002/ajmg.a.62106. Epub 2021 Feb 5. Am J Med Genet A. 2021. PMID: 33544979

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