EurekaMag.com logo
+ Site Statistics
References:
53,869,633
Abstracts:
29,686,251
+ Search Articles
+ Subscribe to Site Feeds
EurekaMag Most Shared ContentMost Shared
EurekaMag PDF Full Text ContentPDF Full Text
+ PDF Full Text
Request PDF Full TextRequest PDF Full Text
+ Follow Us
Follow on FacebookFollow on Facebook
Follow on TwitterFollow on Twitter
Follow on LinkedInFollow on LinkedIn

+ Translate

A 7q21.11 microdeletion presenting with apparent intellectual disability without epilepsy



A 7q21.11 microdeletion presenting with apparent intellectual disability without epilepsy



American Journal of Medical Genetics. Part A 173(4): 1128-1130




(PDF emailed within 0-6 h: $19.90)

Accession: 059298467

Download citation: RISBibTeXText

PMID: 28240412

DOI: 10.1002/ajmg.a.38136



Related references

Ade novo357 Mb microdeletion in 8q123q132 in a patient with mild intellectual disability and epilepsy. 2011

A de novo 3.57 Mb microdeletion in 8q12.3q13.2 in a patient with mild intellectual disability and epilepsy. European Journal of Medical Genetics 55(5): 358-361, 2012

7p22.3 microdeletion disrupting SNX8 in a patient presenting with intellectual disability but no tetralogy of Fallot. American Journal of Medical Genetics. Part A 164a(8): 2133-2135, 2015

RORB gene and 9q21.13 microdeletion: report on a patient with epilepsy and mild intellectual disability. European Journal of Medical Genetics 57(1): 44-46, 2014

15q26.1 microdeletion encompassing only CHD2 and RGMA in two adults with moderate intellectual disability, epilepsy and truncal obesity. European Journal of Medical Genetics 57(9): 520-523, 2015

3p25.3 microdeletion of GABA transporters SLC6A1 and SLC6A11 results in intellectual disability, epilepsy and stereotypic behavior. American Journal of Medical Genetics. Part A 164a(12): 3061-3068, 2015

Maternal complex chromosomal rearrangement leads to TCF12 microdeletion in a patient presenting with coronal craniosynostosis and intellectual disability. American Journal of Medical Genetics. Part A 164a(6): 1530-1536, 2015

Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorder. American Journal of Human Genetics 89(4): 551-563, 2011

Association of Seizure Occurrence with Aneurysm Treatment Modality in Aneurysmal Subarachnoid Hemorrhage Patients. Neurocritical Care, 2018

A novel mutation in GMPPA in siblings with apparent intellectual disability, epilepsy, dysmorphism, and autonomic dysfunction. American Journal of Medical Genetics. Part A 173(8): 2246-2250, 2017

Epilepsy in children with intellectual disability in Bosnia and Herzegovina: effects of sex, level and etiology of intellectual disability. Research in Developmental Disabilities 30(5): 1078-1083, 2009

Ring 21 chromosome presenting with epilepsy and intellectual disability: clinical report and review of the literature. American Journal of Medical Genetics. Part A 155a(4): 911-914, 2011

TCF12 microdeletion in a 72-year-old woman with intellectual disability. American Journal of Medical Genetics. Part A 167a(8): 1897-1901, 2016

8p21 microdeletion in a patient with intellectual disability and behavioral abnormalities. American Journal of Medical Genetics. Part A 155a(12): 3148-3152, 2012

A novel de novo 1.8 Mb microdeletion of 17q21.33 associated with intellectual disability and dysmorphic features. European Journal of Medical Genetics 55(11): 656-659, 2013