Clinical Outcomes and Counselling Issues Regarding Partial Trisomy of Terminal Xp in a Child with Developmental Delay
Author:
Publisher
Sultan Qaboos University Medical Journal
Subject
General Medicine
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Cytogenomic characterization of small supernumerary marker chromosomes in patients with pigmentary mosaicism;Frontiers in Genetics;2024-04-16
2. Patient with Mosaic Turner Syndrome and a Derivative X Chromosome with a Variant Triple X Diagnosis in Fetus: A Case Report;Cytogenetic and Genome Research;2022
3. Genetic and clinical characterization of 73 Pigmentary Mosaicism patients: revealing the genetic basis of clinical manifestations;Orphanet Journal of Rare Diseases;2019-11-15
4. A non-syndromic intellectual disability associated with a de novo microdeletion at 7q and 18p, microduplication at Xp, and 18q partial trisomy detected using chromosomal microarray analysis approach;Molecular Cytogenetics;2014-06-27
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