14qトリソミー
WordNet
- chrosomal abnormality in which there is one more than the normal number of chromosomes in a cell
UpToDate Contents
全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.
English Journal
- [Application of next-generation DNA sequencing for prenatal testing of fetal chromosomal aneuploidies].
- Liu J1, Wang H, Xi H, Jia Z, Zhou Y, Wu L.
- Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.Zhonghua Yi Xue Yi Chuan Xue Za Zhi.2015 Aug;32(4):533-7. doi: 10.3760/cma.j.issn.1003-9406.2015.04.019.
- OBJECTIVE: To explore the value of next-generation sequencing for the non-invasive prenatal testing of fetal chromosomal aneuploidies.METHODS: Plasma from 4004 women with singleton pregnancy at a gestational age between 12-35(+5) weeks was collected prior to amniocentesis between April 19th 2011 and
- PMID 26252102
- Second cancers and Richter transformation are the leading causes of death in patients with trisomy 12 chronic lymphocytic leukemia.
- Strati P1, Abruzzo LV2, Wierda WG1, O'Brien S1, Ferrajoli A1, Keating MJ3.
- Clinical lymphoma, myeloma & leukemia.Clin Lymphoma Myeloma Leuk.2015 Jul;15(7):420-7. doi: 10.1016/j.clml.2015.02.001. Epub 2015 Feb 11.
- BACKGROUND: Trisomy 12 (+12) is detected by fluorescence in-situ hybridization (FISH) analysis in up to 20% of patients with chronic lymphocytic leukemia (CLL). Patients with +12 are known to have unique features and to carry an intermediate prognosis.PATIENTS AND METHODS: In order to better define
- PMID 25800543
- Dermatoglyphics and Reproductive Risk in a Family with Robertsonian Translocation 14q;21q.
- Kolgeci S1, Kolgeci J2, Azemi M2, Daka A3, Shala-Beqiraj R4, Kurtishi I5, Sopjani M5.
- Acta informatica medica : AIM : journal of the Society for Medical Informatics of Bosnia & Herzegovina : časopis Društva za medicinsku informatiku BiH.Acta Inform Med.2015 Jun;23(3):178-83. doi: 10.5455/aim.2015.23.179-183. Epub 2015 May 25.
- AIM: The present study is carried out to evaluate the risk of giving birth to children with Down syndrome in a family with Robertsonian translocation 14q;21q, and to find the dermatoglyphic changes present in carriers of this translocation.METHODS: Cytogenetics diagnosis has been made according to M
- PMID 26236088
Japanese Journal
- 母親由来の第14番染色体による遠位14qトリソミー (Distal 14q trisomy due to a maternal derivative chromosome 14)
- SONODA TOHRU,KOUNO KEIICHIRO,SAWADA KAZUMI,SUGIMOTO TOHRU
- Pediatrics international : official journal of the Japan Pediatric Society 43(3), 313-315, 2001-06-01
- NAID 10010092530
- 14q11 abnormality and trisomy 8q are not common in Japanese T-cell prolymphocytic leukemia
- KOJIMA Kensuke,KOBAYASHI Hajime,IMOTO Shion,NAKAGAWA Toshitaro,MATSUI Toshimitsu,KAWACHI Yosunori,ODA Kenji,YANO Tomofumi,KOBAYASHI Hikaru,NOGUCHI Masaaki,HARA Masamichi,OSHIMI Kazuo
- International journal of hematology 68(3), 291-296, 1998-10
- NAID 10006596173
- 14q11 abnormality and trisomy 8q are not common in Japanese T-cell prolymphocytic leukemia.
Related Links
- Trisomy 14q symptoms, causes, diagnosis, and treatment information for Trisomy 14q (14q+ syndrome) with alternative diagnoses, full-text book chapters, misdiagnosis, research treatments, prevention, and prognosis. ...
- ABSTRACT Trisomy 14q- syndrome is relatively new and needs further delineation. In comparing our case with other reported cases (Table 1), some similarities are seen. Although the comparison of our case of partial trisomy 14 with ...
- Vanessa and Jacob Jennings are brother and sister that share more than blood, they both have Trisomy 14q 32.33, a very rare genetic disorder. So far they are the only known case of it. Contributed by MOM Barbara- Read more ...
★リンクテーブル★
[★]
- 英
- trisomy 14q
- 関
- 14番染色体