WordNet

chromosomal abnormality consisting of the absence of one chromosome from the normal diploid number

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1. 急性骨髄性白血病における細胞遺伝学 cytogenetics in acute myeloid leukemia
2. 血液悪性腫瘍およびリンパ悪性腫瘍の遺伝的異常 genetic abnormalities in hematologic and lymphoid malignancies
3. 骨髄異形成症候群における細胞遺伝学および分子遺伝学 cytogenetics and molecular genetics of myelodysplastic syndromes
4. 血液悪性腫瘍における細胞遺伝子解析の一般的側面 general aspects of cytogenetic analysis in hematologic malignancies
5. 急性骨髄性白血病の分類 classification of acute myeloid leukemia

Unbalanced Translocation der(7)t(7q;11q): A New Recurrent Aberration Leading to Partial Monosomy 7q and Trisomy 11q in Acute Myeloid Leukemia.

Yamamoto K1, Yakushijin K, Miyata Y, Matsuoka H, Minami H.
Acta haematologica.Acta Haematol.2014 May 22;132(2):244-246. [Epub ahead of print]
PMID 24862463

The characteristics and prognostic analysis in 213 myeloid malignancy patients with del(20q): a report of a single-center case series.

Pan J1, Wu C1, Xue Y2, Qiu H1, Chen S1, Zhang J1, Bai S1, Wu Y1, Wang Y1, Shen J1, Gong Y1.
Cancer genetics.Cancer Genet.2014 Mar;207(3):51-6. doi: 10.1016/j.cancergen.2014.02.002. Epub 2014 Feb 13.
The clinical and hematological characteristics and the prognostic significance of del(20q) were investigated in a consecutive series of 213 myeloid malignancies. In the analyses, the cases were divided into three subgroups according to diagnosis or four subgroups according to cytogenetic data. Patie
PMID 24699042

A patient with partial trisomy 21 and 7q deletion expresses mild Down syndrome phenotype.

Papoulidis I1, Papageorgiou E1, Siomou E1, Oikonomidou E1, Thomaidis L2, Vetro A3, Zuffardi O4, Liehr T5, Manolakos E1, Vassilis P6.
Gene.Gene.2014 Feb 25;536(2):441-3. doi: 10.1016/j.gene.2013.11.078. Epub 2013 Dec 13.
BACKGROUND: Down syndrome (DS) is the most common aneuploidy in live-born individuals and it is well recognized with various phenotypic expressions. Although an extra chromosome 21 is the genetic cause for DS, specific phenotypic features may result from the duplication of smaller regions of the chr
PMID 24334122

岡田美智子,宇佐美明美,岡嶋香 [他],三浦裕子,兒玉聖子,志村華絵,田中紀奈,三橋健次郎,石山みどり,風間啓至,吉永健太郎,今井陽一,志関雅幸,森直樹,寺村正尚,泉二登志子,OKADA Michiko,USAMI Akemi,OKAJIMA Kaori,MIURA Hiroko,KODAMA Shoko,SHIMURA Hanae,TANAKA Norina,MITSUHASHI Kenjiro,ISHIYAMA Midori,KAZAMA Hiroshi,YOSHINAGA Kentaro,IMAI Yoichi,SHISEKI Masayuki,MORI Naoki,TERAMURA Masanao,MOTOJI Toshiko
東京女子医科大学雑誌 83(E2), E539-E547, 2013-03-31
… AML-MRCでは、三つ以上の互いに無関係な異常が含まれる複雑核型を有する症例の割合が高く、-5/del(5q), -7/del(7q), +8, -17/del(17p), -20/del(20q)が多くみられた。 …
NAID 110009575063

Monosomy 7 and deletion 7q in children and adolescents with acute myeloid leukemia : an international retrospective study