Familial transmission of 5p13.2 duplication due to maternal der(X)ins(X;5)
Author:
Funder
Wellcome Trust
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference15 articles.
1. Proximal 5p trisomy resulting from a marker chromosome implicates band 5p13 in 5p trisomy syndrome;Avansino;Am J Med Genet,1999
2. Neonatal detection of 5p13.2 duplication and delineation of the phenotype;Carrascosa Romero;Am J Med Genet Part A,2012
3. Trisomy of the short arm of chromosome 5 due to a de novo inversion and duplication (5)(p15.3p13.3);Cervera;Am J Med Genet Part A,2005
4. DECIPHER: database of chromosomal imbalance and phenotype in humans using ensembl resources;Firth;Am J Hum Genet,2009
5. Insertional translocation detected using FISH confirmation of array-comparative genomic hybridization (aCGH) results;Kang;Am J Med Genet Part A,2010
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