Autoradiographic studies on a mother and aborted foetus from a family with four mongoloid children and a presumptive 21-21 translocation.

Suppr

超能文献

作者信息

de Capoa A, Miller O J, Mukherjee B B, Warburton D

出版信息

Ann Hum Genet. 1968 Jan;31(3):243-53. doi: 10.1111/j.1469-1809.1968.tb00555.x.

DOI:10.1111/j.1469-1809.1968.tb00555.x

PMID:4231120

Abstract

摘要

相似文献

Autoradiographic studies on a mother and aborted foetus from a family with four mongoloid children and a presumptive 21-21 translocation.

Ann Hum Genet. 1968 Jan;31(3):243-53. doi: 10.1111/j.1469-1809.1968.tb00555.x.

X chromosome long arm deletion in a patient with Down's syndrome.一名唐氏综合征患者的X染色体长臂缺失。

J Med Genet. 1971 Sep;8(3):387-91. doi: 10.1136/jmg.8.3.387.

DNA replication analysis of six 13-15--21 translocation families.六个13 - 15 - 21易位家族的DNA复制分析。

Ann Hum Genet. 1967 May;30(4):325-8. doi: 10.1111/j.1469-1809.1967.tb00033.x.

Studies on sex-dimorphism of peripheral blood neutrophils in the langdon-down syndrome.关于唐氏综合征外周血中性粒细胞性别二态性的研究。

Pol Med J. 1968;7(5):1130-6.

[Significance of chromosome translocations from the G-D group in the karyotype of the mother of 2 children with Down's syndrome].[2名唐氏综合征患儿母亲核型中G-D组染色体易位的意义]

Pediatr Pol. 1970 Feb;45(2):211-5.

[Functional analysis of chromosome translocation (DqGq) in hereditary Down's syndrome by DNA replication pattern].

Saishin Igaku. 1968 Feb 10;24(2):313-6.

[Cytogenetic studies of families of patients with Down's syndrome].[唐氏综合征患者家庭的细胞遗传学研究]

Tsitologiia. 1966 Mar-Apr;8(2):277-82.

Diverse chromosomal anomalies in a family.一个家族中的多种染色体异常。

J Med Genet. 1968 Dec;5(4):314-8. doi: 10.1136/jmg.5.4.314.

[Incomplete G G translocation in a mongoloid girl].[一名蒙古人种女孩的不完全G G易位]

Folia Clin Int (Barc). 1969 Sep;19(9):448-50.

Human chromosome identification and the pattern of DNA replication in fibroblasts from an XXY male. A quantitative autoradiographic study of early and late synthesis.XXY男性成纤维细胞中的人类染色体鉴定及DNA复制模式。早期和晚期合成的定量放射自显影研究。

Cytogenetics. 1969;8(4):272-95.

引用本文的文献

Cd branding studies in a homologous Robertsonian 13;13 translocation.

J Med Genet. 1982 Aug;19(4):306-10. doi: 10.1136/jmg.19.4.306.

Autoradiographic studies of the human Y chromosome.人类Y染色体的放射自显影研究。

Chromosoma. 1971 Mar 16;32(4):364-77. doi: 10.1007/BF00285250.

The identification of the chromosomes of the F group by quantitative methods, with an appendix on the relative DNA measurements of human chromosomes.用定量方法鉴定F组染色体，并附录人类染色体的相对DNA测量数据。

Humangenetik. 1971;14(1):13-23. doi: 10.1007/BF00273027.

Sibship (21q21q) translocation Down's syndrome with maternal transmission.同胞（21q21q）易位型唐氏综合征伴母系遗传。

J Med Genet. 1973 Dec;10(4):371-5. doi: 10.1136/jmg.10.4.371.

Down's syndrome. Current stage of cytogenetic research.唐氏综合征。细胞遗传学研究的当前阶段。

Humangenetik. 1971;12(1):1-28. doi: 10.1007/BF00291028.

Identification of G group anomalies in Down's syndrome by quinacrine dihydrochloride fluorescence staining.用盐酸阿的平荧光染色法鉴定唐氏综合征中的G组异常。

Humangenetik. 1971;12(1):67-73. doi: 10.1007/BF00291036.

Balanced homologous translocation t(22q22q) in a phenotypically normal woman with repeated spontaneous abortions.一名表型正常但反复自然流产的女性发生平衡同源易位t(22q22q) 。

Humangenetik. 1975 Aug 25;28(4):357-60. doi: 10.1007/BF00284812.

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