Similar articles for PMID: 24801133

Year	Number of Results
1948	1
2004	1
2005	1
2006	3
2007	2
2008	2
2009	5
2010	12
2011	14
2012	23
2013	44
2014	45
2015	21
2016	16
2017	9
2018	13
2019	12
2020	13
2021	14
2022	17
2023	2
2024	0

1

Refinement of the deletion in 8q22.2-q22.3: the minimum deletion size at 8q22.3 related to intellectual disability and epilepsy.

Kuroda Y, Ohashi I, Saito T, Nagai J, Ida K, Naruto T, Iai M, Kurosawa K. Kuroda Y, et al. Am J Med Genet A. 2014 Aug;164A(8):2104-8. doi: 10.1002/ajmg.a.36604. Epub 2014 May 6. Am J Med Genet A. 2014. PMID: 24801133

2

Microdeletion 8q22.2-q22.3 in a 40-year-old male.

Sinajon P, Gofine T, Ingram J, So J. Sinajon P, et al. Eur J Med Genet. 2015 Nov;58(11):569-72. doi: 10.1016/j.ejmg.2015.10.004. Epub 2015 Oct 9. Eur J Med Genet. 2015. PMID: 26455667

3

Five patients with novel overlapping interstitial deletions in 8q22.2q22.3.

Kuechler A, Buysse K, Clayton-Smith J, Le Caignec C, David A, Engels H, Kohlhase J, Mari F, Mortier G, Renieri A, Wieczorek D. Kuechler A, et al. Am J Med Genet A. 2011 Aug;155A(8):1857-64. doi: 10.1002/ajmg.a.34072. Epub 2011 Jul 7. Am J Med Genet A. 2011. PMID: 21739578

4

Interstitial 1q23.3q24.1 deletion in a patient with renal malformation, congenital heart disease, and mild intellectual disability.

Mackenroth L, Hackmann K, Klink B, Weber JS, Mayer B, Schröck E, Tzschach A. Mackenroth L, et al. Am J Med Genet A. 2016 Sep;170(9):2394-9. doi: 10.1002/ajmg.a.37785. Epub 2016 Jun 3. Am J Med Genet A. 2016. PMID: 27255444

5

Deletion of 3p25.3 in a patient with intellectual disability and dysmorphic features with further definition of a critical region.

Kellogg G, Sum J, Wallerstein R. Kellogg G, et al. Am J Med Genet A. 2013 Jun;161A(6):1405-8. doi: 10.1002/ajmg.a.35876. Epub 2013 Apr 23. Am J Med Genet A. 2013. PMID: 23613140

6

Refinement of the critical region of 1q41q42 microdeletion syndrome identifies FBXO28 as a candidate causative gene for intellectual disability and seizures.

Au PY, Argiropoulos B, Parboosingh JS, Micheil Innes A. Au PY, et al. Am J Med Genet A. 2014 Feb;164A(2):441-8. doi: 10.1002/ajmg.a.36320. Epub 2013 Dec 19. Am J Med Genet A. 2014. PMID: 24357076 Review.

7

Chromosome 1q31.2q32.1 deletion in an adult male with intellectual disability, dysmorphic features and obesity.

Hyder Z, Fairclough A, Douzgou S. Hyder Z, et al. Clin Dysmorphol. 2019 Jul;28(3):131-136. doi: 10.1097/MCD.0000000000000281. Clin Dysmorphol. 2019. PMID: 31045593

8

De novo duplication of 17p13.1-p13.2 in a patient with intellectual disability and obesity.

Kuroda Y, Ohashi I, Tominaga M, Saito T, Nagai J, Ida K, Naruto T, Masuno M, Kurosawa K. Kuroda Y, et al. Am J Med Genet A. 2014 Jun;164A(6):1550-4. doi: 10.1002/ajmg.a.36477. Epub 2014 Mar 25. Am J Med Genet A. 2014. PMID: 24668897

9

Interstitial microdeletion of 17q11.2 is associated with hypotonia, fatigue, intellectual disability, and a subtle facial phenotype in three unrelated patients.

Osio D, Rankin J, Koillinen H, Reynolds A, Van Esch H. Osio D, et al. Am J Med Genet A. 2018 Jan;176(1):209-213. doi: 10.1002/ajmg.a.38499. Epub 2017 Nov 12. Am J Med Genet A. 2018. PMID: 29130599

10

A de novo 3.57 Mb microdeletion in 8q12.3q13.2 in a patient with mild intellectual disability and epilepsy.

Verhoeven WM, Egger JI, Feenstra I, de Leeuw N. Verhoeven WM, et al. Eur J Med Genet. 2012 May;55(5):358-61. doi: 10.1016/j.ejmg.2011.10.005. Epub 2011 Nov 27. Eur J Med Genet. 2012. PMID: 22138216

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