A patient with an interstitial deletion of the proximal portion of the long arm of chromosome 4
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference7 articles.
1. B-F Chromosome Translocation Associated with Father-Child Incompatibility within the Gc-System
2. Tentative assignment of piebald trait gene to chromosome band 4q12
3. The child with congenital anomalies and interstitial deletion of the long arm of chromosome 4
Cited by 26 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. Interstitial Deletion 4q due to a Complex Rearrangement Involving Chromosomes 1, 2, 4, 8, 14 and 16;Gazi Medical Journal;2018-07-01
2. 4q12-4q21.21 deletion genotype-phenotype correlation and the absence of piebaldism in presence ofKIThaploinsufficiency;American Journal of Medical Genetics Part A;2014-10-29
3. Array-based characterization of an interstitial de-novo deletion of chromosome 4q in a patient with a neuronal migration defect and hypocalcemia plus a literature review;Clinical Dysmorphology;2012-07
4. Microdeletion at 4q21.3 is associated with intellectual disability, dysmorphic facies, hypotonia, and short stature;American Journal of Medical Genetics Part A;2011-08-10
5. Congenital heart defects in two siblings in an Axenfeld–Rieger syndrome family;Clinical Dysmorphology;2010-04
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