A rare case ofde novo distal 19q trisomy prenatally diagnosed
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference15 articles.
1. First clinical case of small de novo duplication of 19q (13.3-13.4) confirmed by FISH
2. Duplication of distal 19q: Clinical report and review
3. The spatial organization of human chromosomes within the nuclei of normal and emerin-mutant cells
4. Chromosomes are predominantly located randomly with respect to each other in interphase human cells
5. Prenatal detection and molecular characterization of a de novo duplication of the distal long arm of chromosome 19
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1. Prenatal detection and molecular cytogenetic characterization of 19q13.42 microduplication: three reported cases and literature review;Molecular Cytogenetics;2021-01-15
2. De novo unbalanced translocation leading to monosomy 9p24.3p24.1 and trisomy 19q13.42q13.43 characterized by microarray-based comparative genomic hybridization in a child with partial cortical dysplasia and craniofacial dysmorphisms without trigonocephaly;American Journal of Medical Genetics Part A;2013-02-07
3. Familial Subtelomeric Rearrangement of Chromosomes 19 and 20: A New Contribution to Partial Distal 19q Trisomy;Genetic Testing and Molecular Biomarkers;2010-10
4. Monosomy 19pter and trisomy 19q13-qter in two siblings arising from a maternal pericentric inversion: Clinical data and molecular characterization;European Journal of Medical Genetics;2008-11
5. Partial trisomy of distal 19q detected by quantitative real-time PCR and FISH in a girl with mild facial dysmorphism, hypotonia and developmental delay;American Journal of Medical Genetics Part A;2007
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