神经纤维瘤病：前期显带技术未发现染色体缺陷。 - Suppr | 超能文献

Neurofibromatosis: no chromosomal defect by prophase banding technique.

作者信息

Kao Y S, Kao-Shan C S, Knutsen T, Whang-Peng J, Mulvihill J J

出版信息

Cancer Genet Cytogenet. 1984 Nov;13(3):281-2. doi: 10.1016/0165-4608(84)90051-7.

DOI:10.1016/0165-4608(84)90051-7

Abstract

摘要

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验

相似文献

1

Neurofibromatosis: no chromosomal defect by prophase banding technique.神经纤维瘤病：前期显带技术未发现染色体缺陷。

Cancer Genet Cytogenet. 1984 Nov;13(3):281-2. doi: 10.1016/0165-4608(84)90051-7.

2

The many faces of neurofibromatosis.神经纤维瘤病的多样表现

Ariz Med. 1982 Feb;39(2):99-102.

3

A chromosomal survey of an institution for the mentally retarded. Study of 476 karyotypes with banding techniques and clinical assessment of patients with chromosome anomalies.一所智障机构的染色体调查。运用显带技术对476个核型进行研究，并对染色体异常患者进行临床评估。

Dan Med Bull. 1983 Feb;30(1):5-13.

4

[Cytogenetic studies on some rarer dermatoses].[某些罕见皮肤病的细胞遗传学研究]

Hautarzt. 1966 Jan;17(1):35-6.

5

Evidence of chromosomal instability in neurofibromatosis.神经纤维瘤病中染色体不稳定的证据。

Cancer. 1985 May 15;55(10):2434-6. doi: 10.1002/1097-0142(19850515)55:10<2434::aid-cncr2820551022>3.0.co;2-a.

6

Chromosome pattern in juvenile chronic myelogenous leukemia, myelodysplastic syndrome, and acute leukemia associated with neurofibromatosis.

Leukemia. 1989 Jan;3(1):36-41.

7

[Neurofibromatosis and chromosomal translocation. Report of a case of 46, XX,t(2p-:22p+)].[神经纤维瘤病与染色体易位。一例46, XX,t(2p-:22p+)病例报告]

Rev Invest Clin. 1971 Oct-Dec;23(4):311-6.

8

[Ophthalmologic differentiation of various forms of neurofibromatosis].[各种形式神经纤维瘤病的眼科鉴别诊断]

Ophthalmologe. 1993 Aug;90(4):391-3.

9

[Neurofibromatosis I: a clinical series and genetic correlations].

Minerva Pediatr. 1997 Apr;49(4):155-61.

10

Incidence of major chromosomal abnormalities in a referred population for suspected chromosomal aberrations: a report of 357 cases.

Clin Genet. 1980 May;17(5):305-8. doi: 10.1111/j.1399-0004.1980.tb00154.x.

引用本文的文献

1

Cell culture studies on neurofibromatosis (von Recklinghausen). V. Monosomy 22 and other chromosomal anomalies in cultures from peripheral neurofibromas.神经纤维瘤病（冯·雷克林豪森病）的细胞培养研究。V. 来自周围神经纤维瘤培养物中的22号染色体单体及其他染色体异常

Hum Genet. 1986 Dec;74(4):453-5. doi: 10.1007/BF00280506.

2

Chromosomes 17 and 22 involved in marker formation in neurofibrosarcoma in von Recklinghausen disease. A cytogenetic and in situ hybridization study.

Hum Genet. 1990 Aug;85(3):337-42. doi: 10.1007/BF00206758.

3

Genetics of neurofibromatosis 1 in Japan: mutation rate and paternal age effect.日本神经纤维瘤病1型的遗传学：突变率与父亲年龄效应

Hum Genet. 1992 May;89(3):281-6. doi: 10.1007/BF00220540.