1.3 Mb de novo deletion in chromosome band 3q29 associated with normal intelligence in a child
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference10 articles.
1. Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication;Ballif;Mol. Cytogenet.,2008
2. A case of 3q29 microdeletion with novel features and a review of cytogenetically visible terminal 3q deletions;Baynam;Clin. Dysmorphol.,2006
3. 3q29 microdeletion: a mental retardation disorder unassociated with a recognizable phenotype in two mother–daughter pairs;Digilio;Am. J. Med. Genet. A,2009
4. 3q29 interstitial microdeletion syndrome: an inherited case associated with cardiac defect and normal cognition;Li;Eur. J. Med. Genet.,2009
5. Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformations;Rossi;J. Med. Genet.,2001
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1. A distinct cognitive profile in individuals with 3q29 deletion syndrome;Journal of Intellectual Disability Research;2022-03-16
2. A distinct cognitive profile in individuals with 3q29 deletion syndrome;2021-03-08
3. Comprehensive phenotyping of neuropsychiatric traits in a multiplex 3q29 deletion family: a case report;BMC Psychiatry;2020-04-22
4. Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registry;Molecular Autism;2019-07-16
5. A Novel 3q29 Deletion in Association With Developmental Delay and Heart Malformation—Case Report With Literature Review;Frontiers in Pediatrics;2019-07-08
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