Rare proximal interstitial deletion of chromosome 4q, del(4)(q13.2q21.22): New case and comparison with the literature
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference6 articles.
1. Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism;Giebel;Proc Nat Acad Sci,1991
2. Severe mental retardation and mild dysmorphism: Association with an uncommon interstitial deletion of chromosome 4;Mascari;Am H Hum Genet,1989
3. Partial monosomy of long arm of chromosome due to interstitial deletion;McDemort;Hum Genet,1980
4. Deletion 4q21/4q22 syndrome: Two patients with de novo 4q21.3q23 and 4q13.2q23 deletions;Nowaczyk;Am J Med Genet,1997
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1. Outcomes of two different unbalanced segregations from a maternal t(4;10)(q33;p15.1) translocation;BMC Medical Genomics;2023-03-29
2. Deletion of 4q13.2q21.1 chromosome and autism spectrum disorder;Journal of Pediatric Neurosciences;2022
3. Interstitial Deletion 4q due to a Complex Rearrangement Involving Chromosomes 1, 2, 4, 8, 14 and 16;Gazi Medical Journal;2018-07-01
4. Interstitial microdeletions including the chromosome band 4q13.2 and theUBA6gene as possible causes of intellectual disability and behavior disorder;American Journal of Medical Genetics Part A;2015-08-18
5. Microdeletions of 5.5 Mb (4q13.2-q13.3) and 4.1 Mb (7p15.3-p21.1) associated with a saethre-chotzen-like phenotype, severe intellectual disability, and autism;American Journal of Medical Genetics Part A;2013-07-04
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