Further contribution to the description of phenotypes associated with partial 4q duplication
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference17 articles.
1. Partial trisomy 4q due to familial 2/4 translocation
2. Partial trisomy 4q: Two cases resulting from a familial translocation t(4;18)(q27;p11)
3. Partial trisomy 4q syndrome: Case report and review
4. Patterns of acrorenal malformation associations
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2. A Case of Inherited t(4;10)(q26;q26.2) Chromosomal Translocation Elucidated by Multiple Chromosomal and Molecular Analyses. Case Report and Review of the Literature;Genes;2021-12-07
3. Cytogenetic and molecular analysis of distal 4q duplication with distinctive phenotype using single-nucleotide polymorphism array;Molecular Cytogenetics;2021-09-29
4. Prenatal diagnosis of de novo small supernumerary marker chromosome 4q (4q11-q12): A case report;International Journal of Reproductive BioMedicine (IJRM);2021-06-23
5. Autism spectrum disorder in a patient with a genomic rearrangement that only involves the EPHA5 gene;Psychiatric Genetics;2019-06
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