De novo interstitial deletion of 11q14.3q22 in a boy with mild intellectual disability and short stature
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Genetics (clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology and Child Health
Reference13 articles.
1. Familial deletion 11q14.3-q22.1 without apparent phenotypic consequences: a haplosufficient 8.5 Mb region.;Goumy;Am J Med Genet A,2008
2. 11q14.1-11q22.1 deletion in a 1-year-old male with minor dysmorphic features.;Kariminejad;Am J Med Genet A,2010
3. Directly Transmitted 12.3-Mb Deletion with a Consistent Phenotype in the Variable 11q21q22.3 Region.;Kirk;Cytogenet Genome Res,2020
4. A large interstitial 11q deletion with isolated mild intellectual disability: review of the literature for genotype-phenotype correlation.;Lallar;Clin Dysmorphol,2018
5. Identification of a haplosufficient 3.6-Mb region in human chromosome 11q14.3–>q21.;Li;Cytogenet Genome Res,2002
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