首页> 外文OA文献 >Bovine exome sequence analysis and targeted SNP genotyping of recessive fertility defects BH1, HH2, and HH3 reveal a putative causative mutation in SMC2 for HH3.

【2h】

Bovine exome sequence analysis and targeted SNP genotyping of recessive fertility defects BH1, HH2, and HH3 reveal a putative causative mutation in SMC2 for HH3.

机译：牛外显子组序列分析和隐性生育缺陷BH1，HH2和HH3的靶向sNp基因分型揭示了smC2中HH3的推定致病突变。

代理获取

本网站仅为用户提供外文OA文献查询和代理获取服务，本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文，但由于OA文献来源多样且变更频繁，仍可能出现获取不到、文献不完整或与标题不符等情况，如果获取不到我们将提供退款服务。请知悉。

页面导航

著录项
相似文献
相关主题

著录项

作者
Matthew C McClure; Derek Bickhart; Dan Null; Paul Vanraden; Lingyang Xu; George Wiggans; George Liu; Steve Schroeder; Jarret Glasscock; Jon Armstrong; John B Cole; Curtis P Van Tassell; Tad S Sonstegard;
展开▼
作者单位

展开▼
年度 2014
总页数
原文格式 PDF
正文语种
中图分类

相似文献

外文文献

1. Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia [J] . E Rees, G Kirov, J T Walters, Translational psychiatry. . 2015,第7期

机译：604例三重性精神分裂症隐性基因型的外显子组序列分析
2. Whole-exome sequence analysis highlights the role of unmasked recessive mutations in copy number variants with incomplete penetrance [J] . Egloff Matthieu, Nguyen Lam-Son, Siquier-Pernet Karine, European journal of human genetics: EJHG . 2018,第6a6期

机译：全极端序列分析突出了未完全渗透的拷贝数变体中未掩蔽的隐性突变的作用
3. Exome sequence analysis of Kaposiform hemangioendothelioma: identification of putative driver mutations * [J] . Sho Egashira, Satoshi Fukushima, Masatoshi Jinnin, Anais Brasileiros de Dermatologia . 2016,第6期

机译：Kaposiform血管内皮瘤的外显子组序列分析：推定的驱动子突变的鉴定*
4. Bovine Exome Sequence Analysis and Targeted SNP Genotyping of Recessive Fertility Defects BH1 HH2 and HH3 Reveal a Putative Causative Mutation in SMC2 for HH3 [O] . Matthew C. McClure, Derek Bickhart, Dan Null, -1

机译：牛外显子组序列分析和隐性育性缺陷BH1HH2和HH3的靶向SNP基因分型揭示了SMC2中HH3的假定致病突变。
5. Whole genome SNP genotyping and exome sequencing reveal novel genetic variants and putative causative genes in congenital hyperinsulinism. [O] . Maria Carla Proverbio, Eleonora Mangano, Alessandra Gessi, 2013

机译：全基因组sNp基因分型和外显子组测序揭示了先天性高胰岛素血症中的新型遗传变异和推定的致病基因。

Bovine exome sequence analysis and targeted SNP genotyping of recessive fertility defects BH1, HH2, and HH3 reveal a putative causative mutation in SMC2 for HH3.

著录项

相似文献

相关主题

期刊订阅