Deletion of 2p: A cytogenetic and clinical update
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference9 articles.
1. Report of the committee on the genetic constitution of chromosomes 2, 3, 4, and 5
2. Deletion mapping: Further evidence for the location of acid phosphatase (ACP1) within 2p23
3. Assignment by Deletion of Human Red Cell Acid Phosphatase Gene Locus to the Short Arm of Chromosome 2
4. Regional assignment of red cell acid phosphatase locus to band 2p25
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1. Diffuse Pediatric-Type High-Grade Glioma H3-/IDH-wildtype with MYCN Deletion and Constitutional Mismatch Repair Deficiency: Case Presentation;Archives of Case Reports;2023-10-26
2. Features of Feingold syndrome 1 dominate in subjects with 2p deletions including MYCN;American Journal of Medical Genetics Part A;2018-08-08
3. PTRHD1(C2orf79) mutations lead to autosomal-recessive intellectual disability and parkinsonism;Movement Disorders;2016-10-18
4. Further phenotype description, genotype characterization in patients with de novo interstitial deletion on 2p23.2-24.1;American Journal of Medical Genetics Part A;2014-04-03
5. Molecular cytogenetic characterization of 2p23.2p23.3 deletion in a child with developmental delay, hypotonia and cryptorchism;European Journal of Medical Genetics;2013-01
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