A rare case: mosaic trisomy 22
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference17 articles.
1. Clinical and molecular studies in full trisomy 22: further delineation of the phenotype and review of the literature;Bacino;Am. J. Med. Genet.,1995
2. Prenatal confirmation of true fetal trisomy 22 mosaicism by fetal skin biopsy following normal fetal blood sampling;Berghella;Prenat. Diagn.,1998
3. Mosaic trisomy 22: a case presentation and literature review of trisomy 22 phenotypes;Crowe;Am. J. Med. Genet.,1997
4. Unilateral radial aplasia and trisomy 22 mosaicism;Dulitzky;J. Med. Genet.,1981
5. Full trisomy 22 in a malformed newborn female;Feret;Ann. Genet.,1991
Cited by 9 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. Trisomy 22 Mosaicism from Prenatal to Postnatal Findings: A Case Series and Systematic Review of the Literature;Genes;2024-03-08
2. Occurrence of mosaic trisomy 22 and pericentric inversion of chromosome 9 in a patient with a good prognosis;BMC Medical Genomics;2023-11-13
3. Mosaic trisomy 22 in a 4-year-old boy with congenital heart disease and general hypotrophy: A case report;Journal of Clinical Laboratory Analysis;2018-09-26
4. Trisomy 22 Mosaicism and Normal Developmental Outcome: Report of Two Patients and Review of the Literature;American Journal of Medical Genetics Part A;2013-03-25
5. Detection of mosaicism for genome imbalance in a cohort of 3,042 clinical cases using an oligonucleotide array CGH platform;European Journal of Medical Genetics;2011-03
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