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chrosomal abnormality in which there is one more than the normal number of chromosomes in a cell

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1. 先天性の細胞遺伝学的異常 congenital cytogenetic abnormalities
2. 血管免疫芽球性Ｔ細胞性リンパ腫の臨床症状、病理学的特徴、および診断 clinical manifestations pathologic features and diagnosis of angioimmunoblastic t cell lymphoma
3. 先天性横隔膜ヘルニア：出生前診断およびマネージメント congenital diaphragmatic hernia prenatal diagnosis and management
4. 胎児異数性に関連する超音波所見 sonographic findings associated with fetal aneuploidy
5. 多発性骨髄腫における病期分類および予後研究 staging and prognostic studies in multiple myeloma

Chromosome 21-derived hsa-miR-155-5p regulates mitochondrial biogenesis by targeting Mitochondrial Transcription Factor A (TFAM).

Quiñones-Lombraña A1, Blanco JG2.
Biochimica et biophysica acta.Biochim Biophys Acta.2015 Jul;1852(7):1420-7. doi: 10.1016/j.bbadis.2015.04.004. Epub 2015 Apr 11.
The regulation of mitochondrial biogenesis is under the control of nuclear genes including the master Mitochondrial Transcription Factor A (TFAM). Recent evidence suggests that the expression of TFAM is regulated by microRNAs (miRNAs) in various cellular contexts. Here, we show that hsa-miR-155-5p,
PMID 25869329

MicroRNA-194-5p could serve as a diagnostic and prognostic biomarker in myelodysplastic syndromes.

Choi JS1, Nam MH1, Yoon SY1, Kang SH2.
Leukemia research.Leuk Res.2015 Jul;39(7):763-8. doi: 10.1016/j.leukres.2015.04.013. Epub 2015 Apr 25.
Trisomy 8 and trisomy 1q are the most frequent chromosomal abnormalities in Korean patients with myelodysplastic syndrome (MDS). MicroRNA (miRNA) deregulation is involved in the development of hematological malignancies, including MDS, and cancer-associated genomic regions are known to encode miRNAs
PMID 25975751

Walters-Sen LC1, Windemuth K1, Angione K1, Nandhlal J1, Milunsky JM2.
European journal of medical genetics.Eur J Med Genet.2015 May;58(5):305-9. doi: 10.1016/j.ejmg.2015.03.004. Epub 2015 Apr 6.
Submicroscopic duplications of 5p13 have been recently reported in several cases, warranting the description of a new clinical entity (Chromosome 5p13 Duplication Syndrome; MIM 613174). These microduplications, while variable in size, all contain at least part of the NIPBL gene. Patients with duplic
PMID 25858703

P1-IS-53 Prenatal 3D-ultrasound diagnosis of Exencephaly associated with partial trisomy 2p and distal 5p deletion

Kim Sa Jin,Kim Min Jeong,Kim Myung Shin,Park In Yang,Hur Soo Young,Lee Gui Sera,Shin Joung Chul
日本産科婦人科學會雜誌 59(2), 775, 2007-02-01
NAID 110006804439

Stillborn baby with partial monosomy of the short arm of chromosome 5 and partial trisomy of the short arm of chromosome 20

OKADA Michiko,USAMI Akemi,OKAJIMA Kaori,YAMADA Miwako,YAMAGUCHI Yuka,UMEZAKI Izumi,MATSUDA Yoshio,OHTA Hiroaki
Congenital anomalies 45(4), 161-164, 2005-12-01
NAID 10027384697

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