Distal deletion, del(2)(q33.3q33.3), in a patient with severe growth deficiency and minor anomalies
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference9 articles.
1. Interstitial deletion 2q33.3-q34 in a boy with a phenotype resembling the Seckel syndrome
2. Interstitial deletion of the long arm of chromosome 2 with normal levels of isocitrate dehydrogenase.
3. Del(2q) - cause of the wrinkly skin syndrome?
4. Interstitial deletion of chromosome 2.
5. Interstitial deletion 2q32.1----q34 in a child with half normal activity of ribulose 5-phosphate 3-epimerase (RPE).
Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Autistic and Rett-like features associated with 2q33.3-q34 interstitial deletion;American Journal of Medical Genetics Part A;2015-04-21
2. Deletion of 4.4 Mb at 2q33.2q33.3 May Cause Growth Deficiency in a Patient with Mental Retardation, Facial Dysmorphic Features and Speech Delay;Cytogenetic and Genome Research;2015
3. A fetus with de novo 2q33.2q35 deletion including MAP2 with brain anomalies, esophageal atresia, and laryngeal stenosis;American Journal of Medical Genetics Part A;2013-11-15
4. Ectodermal dysplasia-like syndrome with mental retardation due to contiguous gene deletion: Further clinical and molecular delineation of del(2q32) syndrome;American Journal of Medical Genetics Part A;2009-12-23
5. Autistic and dysmorphic features associated with a submicroscopic 2q33.3–q34 interstitial deletion detected by array comparative genomic hybridization;American Journal of Medical Genetics Part A;2008
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