Clinical and molecular cytogenetic characterization of four patients with unbalanced translocation der(1)t(1;22)(p36;q13)
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference22 articles.
1. Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: Is less more?;Bejjani;Am J Med Genet Part A,2005
2. Two successive partial trisomies for opposite halves of chromosome 22 in a mother with a balanced translocation;Bendel;J Med Genet,1982
3. Cryptic duplication of the distal segment of 22q due to a translocation (21;22): Three case reports and a review of the literature;Feenstra;Eur J Med Genet,2006
4. Partial duplication of the long arm of chromosome 22 (22q 13) with complete 22 trisomy phenotype;Fryns;Acta Paediatr Belg,1980
5. Identification of cryptic imbalance in phenotypically normal and abnormal translocation carriers;Gajecka;Eur J Hum Genet,2006
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3. Unexpected complexity at breakpoint junctions in phenotypically normal individuals and mechanisms involved in generating balanced translocations t(1;22)(p36;q13);Genome Research;2008-09-02
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