5p13 microduplication in a malformed fetus and his unaffected father
Author:
Affiliation:
1. Kariminejad‐Najmabadi Pathology and Genetics Center Tehran Iran
2. Department of Pediatrics Amsterdam UMC, University of Amsterdam Amsterdam The Netherlands
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.63030
Reference27 articles.
1. Proximal 5p trisomy resulting from a marker chromosome implicates band 5p13 in 5p trisomy syndrome
2. Neonatal detection of 5p13.2 duplication and delineation of the phenotype
3. Trisomy of the short arm of chromosome 5 due to a de novo inversion and duplication (5)(p15.3 p13.3)
4. A copy number variation morbidity map of developmental delay
5. DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources
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