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多发性内分泌腺瘤病2型(MEN-II)中一种拟议的间质性20号染色体短臂12.2区缺失(del(20p12.2))的定量研究

Quantitative study of a proposed interstitial del (20p 12.2) in multiple endocrine neoplasia (MEN-II).

作者信息

Krizman D B, Pathak S, Samaan N A, Chong J L, Hickey R C

出版信息

Anticancer Res. 1986 Mar-Apr;6(2):191-4.

PMID:2871802
Abstract

A quantitative measurement of the prophase Giemsa banding patterns in chromosome 20 of the peripheral blood samples obtained from seven patients with medullary carcinoma of the thyroid (MCT), three nonsymptomatic family members of MCT patients, and three normal controls has revealed no differences in the short arms of the two homologs. More specifically, measurements of band from 20p 12.1 to 20p 12.3 and statistical analysis of the mean ratio between these bands have given no indication of intersitial deletion in chromosome 20p of MCT patients.

摘要

对取自7例甲状腺髓样癌(MCT)患者、3例MCT患者无症状家庭成员及3名正常对照者的外周血样本中20号染色体前期吉姆萨带型进行的定量测量显示,两条同源染色体短臂无差异。更具体地说,对20p12.1至20p12.3区域条带的测量以及这些条带间平均比率的统计分析未显示MCT患者20号染色体短臂存在中间缺失迹象。

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