Long-term follow-up of a 26-year-old male with duplication of 16p: Clinical report and review
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference35 articles.
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3. Chromosome anomalies as a cause of spontaneous abortion
4. De novo trisomy 16p
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1. A pure de novo 16p13.3 duplication and amplification in a patient with femoral hypoplasia, psychomotor retardation, heart defect, and facial dysmorphism—a case report and literature review of the partial 16p13.3 trisomy syndrome;Journal of Applied Genetics;2022-12-31
2. A rare description of pure partial trisomy of 16q12.2q24.3 and review of the literature;American Journal of Medical Genetics Part A;2021-06
3. An Indian infant with de novo duplication of 16p chromosome: A rare genetic syndrome;Indian Journal of Medical Sciences;2020-12-22
4. Mosaic Trisomy 16 Associated with Left Lung Agenesis, Abnormal Left Arm, and Right Pulmonary Artery Stenosis: Expanding the Phenotype and Review of the Literature;Journal of Pediatric Genetics;2020-11-23
5. 16p13 microduplication without CREBBP involvement: Moving toward a phenotype delineation;European Journal of Medical Genetics;2017-03
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