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视网膜母细胞瘤患者及其家族中13号染色体14区带缺失的发生率及意义。

Incidence and significance of a deletion of chromosome band 13q14 in patients with retinoblastoma and in their families.

作者信息

Liberfarb R M, Bustos T, Miller W A, Sang D

出版信息

Ophthalmology. 1984 Dec;91(12):1695-9. doi: 10.1016/s0161-6420(84)34090-8.

Abstract

Ten unrelated retinoblastoma patients were studied cytogenetically with high-resolution prophase banding; two had a deletion of chromosome 13, band q14. Neither of the two patients had any of the congenital defects usually associated with 13q14 deletions. In patient A, the deletion was found to be de novo. Patient B was found to be mosaic for the 13q14 deletion with 54% of the lymphocytes examined having the deletion. This study indicates that the 13q14 deletion may occur in a significant portion of all retinoblastoma cases. Esterase D activity and isozymes were studied also. The significance of findings will be discussed.

摘要

对10名无亲缘关系的视网膜母细胞瘤患者进行了高分辨率前期带型细胞遗传学研究;其中2名患者存在13号染色体q14带缺失。这两名患者均没有通常与13q14缺失相关的任何先天性缺陷。在患者A中,发现该缺失是新发的。发现患者B为13q14缺失的嵌合体,所检测的淋巴细胞中有54%存在该缺失。这项研究表明,13q14缺失可能在所有视网膜母细胞瘤病例中占相当大的比例。还研究了酯酶D活性和同工酶。将对研究结果的意义进行讨论。

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