Unbalanced 3;22 translocation with 22q11 and 3p deletion syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.33249/fullpdf
Reference27 articles.
1. CALL gene is haploinsufficient in a 3p- syndrome patient;Angeloni;Am J Med Genet part A,1999
2. DiGeorge/velocardiofacial syndrome: FISH studies of chromosomes 22q11 and 10p14, and clinical reports on the proximal 22q11 deletion;Bartsch;Am J Med Genet Part A,2003
3. Ocular findings in children with a microdeletion in chromosome 22q11.2;Casteels;Eur J Pediatr,2008
4. Involvement of a palindromic chromosome 22-specific low-copy repeat in a constitutional t(X; 22) (q27;q11);Debeer;Clin Genet,2002
5. AT-rich palindromes mediate the constitutional t(11;22) translocation;Edelmann;Am J Hum Genet,2001
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1. Case Report: A Case Report and Literature Review of 3p Deletion Syndrome;Frontiers in Pediatrics;2021-02-10
2. Distal 3p Duplication and 22q13.3 Deletion with Severe Hypotonia Originating from a Paternal Balanced Translocation (3;22);Molecular Syndromology;2020
3. De novo Unbalanced 1;22 Translocation with 22q11 Deletion Syndrome;Cytogenetic and Genome Research;2019
4. De novo unbalanced translocation t(15;22)(q26.2;q12) with velo‑cardio‑facial syndrome: A case report and review of the literature;Experimental and Therapeutic Medicine;2018-08-16
5. An 18.3-Mb Duplication on Chromosome 14q With Multiple Cardiac Anomalies and Clubfoot Was Identified by Microarray Analysis;Annals of Laboratory Medicine;2016-03-01
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