Molecular cytogenetic characterization and origin of two de novo duplication 9p cases
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference22 articles.
1. A New Case of Trisomy for the Short Arm of No. 9 Chromosome
2. Possible intrachromosomal duplication in a case of trisomy 9p
3. Duplication of the short arm of chromosome 9. Analysis of five cases
4. Partial duplication of the short arm of chromosome 9 (p13→p22) in a child with typical 9p trisomy phenotype
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1. A de novo chromosome 9p duplication in a female child with short stature and developmental delay;SAGE Open Medical Case Reports;2023-01
2. A de novo partial trisomy 9p with Dandy–Walker malformation and ventriculomegaly;Taiwanese Journal of Obstetrics and Gynecology;2022-11
3. Prenatal diagnosis of maternal partial trisomy 9p23p24.3 and 14q11.2q21.3 in a fetus: a case report;Molecular Cytogenetics;2020-02-06
4. De Novo Duplication of Chromosome 9p in a Female Infant: Phenotype and Genotype Correlation;Journal of Pediatric Genetics;2019-09-16
5. Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9;Taiwanese Journal of Obstetrics and Gynecology;2017-08
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