Simple, rapid nonradioactive method to detect major cystic fibrosis mutations in Ashkenazi Jews. - Suppr | 超能文献

Simple, rapid nonradioactive method to detect major cystic fibrosis mutations in Ashkenazi Jews.

作者信息

Avidor B, Zakut H, Kerem B

机构信息

Dept. of Obstet. and Gynecol., Sackler Faculty of Med., Tel Aviv Univ., Edith Wolfson Med. Center, Holon, Israel.

出版信息

Clin Chem. 1996 Jan;42(1):103-5.

Abstract

摘要

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

文档翻译

学术文献翻译模型，支持多种主流文档格式。

相似文献

1

Simple, rapid nonradioactive method to detect major cystic fibrosis mutations in Ashkenazi Jews.

Clin Chem. 1996 Jan;42(1):103-5.

2

Cystic fibrosis in Jews: frequency and mutation distribution.犹太人中的囊性纤维化：发病率及突变分布

Genet Test. 1997;1(1):35-9. doi: 10.1089/gte.1997.1.35.

3

Cystic fibrosis heterozygote screening in the Orthodox Community of Ashkenazi Jews: the Dor Yesharim approach and heterozygote frequency.阿什肯纳兹犹太教正统社区的囊性纤维化杂合子筛查：多雷沙林方法与杂合子频率

Eur J Hum Genet. 1996;4(6):338-41. doi: 10.1159/000472229.

4

Dynamic modification strategy of the Israeli carrier screening protocol: inclusion of the Oriental Jewish Group to the cystic fibrosis panel.以色列携带者筛查方案的动态调整策略：将东方犹太人群纳入囊性纤维化检测组。

Genet Med. 2009 Feb;11(2):101-3. doi: 10.1097/GIM.0b013e31818efd59.

5

Difference in frequencies of the cystic fibrosis alleles, delta F508 and W1282X, between carriers and patients.携带者与患者之间囊性纤维化等位基因（ΔF508和W1282X）频率的差异。

Eur J Hum Genet. 1994;2(2):77-82. doi: 10.1159/000472347.

6

Cystic fibrosis mutations delta F508 and G542X in Jewish patients.犹太患者中的囊性纤维化突变ΔF508和G542X

J Med Genet. 1992 Feb;29(2):131-3. doi: 10.1136/jmg.29.2.131.

7

Population-specific screening by mutation analysis for diseases frequent in Ashkenazi Jews.通过突变分析对阿什肯纳兹犹太人中常见疾病进行特定人群筛查。

Hum Mutat. 1996;8(2):116-25. doi: 10.1002/(SICI)1098-1004(1996)8:2<116::AID-HUMU3>3.0.CO;2-9.

8

Highly variable incidence of cystic fibrosis and different mutation distribution among different Jewish ethnic groups in Israel.以色列不同犹太族群中囊性纤维化的发病率差异很大，且突变分布不同。

Hum Genet. 1995 Aug;96(2):193-7. doi: 10.1007/BF00207378.

9

A new mutation in the CFTR gene, composed of two adjacent DNA alterations, is a common cause of cystic fibrosis among Georgian Jews.

Genomics. 1993 Jan;15(1):236-7. doi: 10.1006/geno.1993.1046.

10

Detection of multiple cystic fibrosis mutations by reverse dot blot hybridization: a technology for carrier screening.

Hum Genet. 1992 May;89(2):163-8. doi: 10.1007/BF00217117.

引用本文的文献

1

Cat scratch disease: the rare role of Afipia felis.猫抓病：阿菲披亚菌属在其中的罕见作用

J Clin Microbiol. 1998 Sep;36(9):2499-502. doi: 10.1128/JCM.36.9.2499-2502.1998.

2

Molecular diagnosis of cat scratch disease: a two-step approach.猫抓病的分子诊断：一种两步法。

J Clin Microbiol. 1997 Aug;35(8):1924-30. doi: 10.1128/jcm.35.8.1924-1930.1997.