Identification of a novel B allele with multiple missense mutations in a Chinese family with a Bw phenotype

Yang Xiaojun; Xie Haihua; Chen Liangyuan; Lin Haibin; Chen Fawen

首页> 外文期刊>Transfusion: The Journal of the American Association of Blood Banks >Identification of a novel B allele with multiple missense mutations in a Chinese family with a Bw phenotype

【24h】

Identification of a novel B allele with multiple missense mutations in a Chinese family with a Bw phenotype

机译：用BW表型在中国家庭中具有多种畸形突变的新型B等位基因的鉴定

获取原文

获取原文并翻译 | 示例

获取外文期刊封面封底 >>

开具论文收录证明 >>

文献代查 >>

团队文献服务 >>

页面导航

著录项
相似文献
相关主题

著录项

来源
《Transfusion: The Journal of the American Association of Blood Banks 》 |2018年第11期| 共2页
作者
Yang Xiaojun; Xie Haihua; Chen Liangyuan; Lin Haibin; Chen Fawen;
展开▼
作者单位

Department of Transfusion MedicineClinical College of Fujian Provincial Hospital Fujian Medical;

Department of Transfusion MedicineFujian Provincial Jinshan HospitalFuzhou Fujian China;

Department of Transfusion MedicineClinical College of Fujian Provincial Hospital Fujian Medical;

Department of Transfusion MedicineFujian Provincial Jinshan HospitalFuzhou Fujian China;

Department of Transfusion MedicineClinical College of Fujian Provincial Hospital Fujian Medical;

展开▼
收录信息
原文格式 PDF
正文语种 eng
中图分类治疗学 ;
关键词

相似文献

外文文献
中文文献
专利

1. Identification of a novel B allele with multiple missense mutations in a Chinese family with a Bw phenotype [J] . Yang Xiaojun, Xie Haihua, Chen Liangyuan, Transfusion: The Journal of the American Association of Blood Banks . 2018 ,第11期

机译：用BW表型在中国家庭中具有多种畸形突变的新型B等位基因的鉴定
2. Identification of a novel missense mutation (p.Ser230Asn) in RHD RHD allele in a Chinese individual with partial D phenotype [J] . Zhang Jingwei, Guo Ming, Tian Li Transfusion: The Journal of the American Association of Blood Banks . 2018 ,第7期

机译：用部分d表型在中国个体中rhD RHD等位基因中的新型畸形突变（P.SER230ASN）
3. A novel A allele with multiple missense mutations in Exon 7 identified in a Chinese individual [J] . Hou Li, Tian Li Transfusion: The Journal of the American Association of Blood Banks . 2016 ,第3期

机译：在中国人中发现的新型Exon 7中具有多个错义突变的A等位基因
4. Identification of fad2 mutations and development of Allele-Specific Markers for High Oleic acid content in rapeseed (Brassica napus L.) [C] . Falentin Cyril, Brégeon Michel, Lucas Marie-Odile, Proceedings of the 12th International Rapeseed Congress: Sustainable Development in Cruciferous Oilseed Crops Production . 2007

机译：fad2突变的鉴定和油菜籽中高油酸含量的等位基因特异性标记的开发（甘蓝型油菜）
5. Functional studies of rare CFTR missense mutations facilitate interpretation of genotype-phenotype relationships. [D] . Krasnov, Kristina V. 2009

机译：罕见CFTR错义突变的功能研究有助于解释基因型与表型的关系。
6. Phenotype of Usher syndrome type II assosiated with compound missense mutations of c.721 CT and c.1969 CT in MYO7A in a Chinese Usher syndrome family [O] . Wei Zhai, Xin Jin, Yan Gong, 2015

机译：与中国Usher综合征家族中MYO7A中c.721 C T和c.1969 C T的复合错义突变相关的II型Usher综合征的表型
7. A prospective study of brachytelephalangic chondrodysplasia punctata: identification of arylsulfatase E mutations, functional analysis of novel missense alleles, and determination of potential phenocopies [O] . Claudia Matos-Miranda, Graeme Nimmo, Bradley Williams, 2013

机译：Brachytelephalangic chondrodysplasia punctata的前瞻性研究：芳基硫酸酶E突变的鉴定，新颖的畸形等位基因的功能分析，以及潜在的斑缺失的测定

Identification of a novel B allele with multiple missense mutations in a Chinese family with a Bw phenotype

著录项

相似文献

相关主题

期刊订阅