Duplication of 5q15-q23.2: Case report and literature review
Author:
Publisher
Wiley
Subject
Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology, and Child Health
Reference19 articles.
1. Distal 5q trisomy resulting from an X;5 translocation detected by chromosome painting
2. Familial insertion (3;5)(q25.3;q22.1q31.3) with deletion or duplication of chromosome region 5q22.1-5q31.3 in ten unbalanced carriers
3. Paternal duplication of chromosome 5q11.2–5q14 in a male born with craniostenosis, ear tags, kidney dysplasia and several other anomalies
4. Balanced rearrangement of chromosomes 2, 5, and 13 in a family with duplication 5q and fetal loss
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1. Healthy Genetically Normal Live-Birth After Mosaic Chromosome 5 Embryo Transfer: A Case Report;Fertility & Reproduction;2021-02-05
2. Prenatal diagnosis of a 5q35.3 microduplication involving part of the ADAMTS2 locus: a likely benign variant without apparent phenotypic abnormality;Medicine;2019-12
3. A Small Supernumerary Marker Derived from the Pericentromeric Region of Chromosome 5: Case Report and Delineation of Partial Trisomy 5p Phenotype;Cytogenetic and Genome Research;2017
4. Chromosome 5 derived small supernumerary marker: towards a genotype/phenotype correlation of proximal chromosome 5 imbalances;Journal of Applied Genetics;2011-03-25
5. De-novo duplication of 5(q13.3q21.1) in a child with vitreo-retinal dysplasia and learning disability;Clinical Dysmorphology;2010-04
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