Vol 93, No 11 (2022)
Clinical vignette
Published online: 2022-03-01
Prenatal diagnosis of chromosome 3q25.32 and 12p11.22p11.1 microduplication with a favorable outcome
Abstract
Not available
Keywords: microduplicationchromosomal microarray analysisprenatal diagnosis
References
- Watson CT, Marques-Bonet T, Sharp AJ, et al. The genetics of microdeletion and microduplication syndromes: an update. Annu Rev Genomics Hum Genet. 2014; 15: 215–244.
- Chen CP, Chern SR, Chen YN, et al. Mosaic trisomy 15 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review. Taiwan J Obstet Gynecol. 2015; 54(4): 426–431.
- Youssef EM, Chen Xq, Higuchi E, et al. Hypermethylation and silencing of the putative tumor suppressor Tazarotene-induced gene 1 in human cancers. Cancer Res. 2004; 64(7): 2411–2417.
- Zhang J, Liu L, Pfeifer GP. Methylation of the retinoid response gene TIG1 in prostate cancer correlates with methylation of the retinoic acid receptor beta gene. Oncogene. 2004; 23(12): 2241–2249.
- Kloth M, Goering W, Ribarska T, et al. The SNP rs6441224 influences transcriptional activity and prognostically relevant hypermethylation of RARRES1 in prostate cancer. Int J Cancer. 2012; 131(6): E897–E904.
- Zhang H, Xi Qi, Liu X, et al. Prenatal Diagnosis and Molecular Cytogenetic Characterization of Copy Number Variations on 4p15.2p16.3, Xp22.31, and 12p11.1q11 in a Fetus with Ultrasound Anomalies: A Case Report and Literature Review. Biomed Res Int. 2020; 2020: 1761738.
