Eur J Med Genet -

A new mutation for Huntington disease following maternal transmission of an intermediate allele. Eur J Med Genet. 2015 Jan;581:28-30. Authors: Semaka A, Kay C, Belfroid RD, Bijl. Redirected from Eur J Med Genet The European Journal of Medical Genetics is a monthly peer-reviewed medical journal covering medical genetics in human and experimental systems. It was established in 1958 as Annales de Génétique, obtaining its current name in 2005. 2019/12/21 · Table of Contents 2018 - 61 10 Is it research or is it clinical? Revisiting an old frontier through the lens of next-generation sequencing technologies. October 01, 2018 [ MEDLINE Abstract] Auto-immune disorders in a. 影响因子官网,提供SCI期刊EUR J MED GENET,EUROPEAN JOURNAL OF MEDICAL GENETICS1769-72122000-2014,2015及历年影响因子impactfactor,专业排名,论文被引频次,论文收录等专业数据查询.

2019 - 62 12 Oro-dental and cranio-facial characteristics of osteogenesis imperfecta type V. December 01, 2019 [ MEDLINE Abstract] Hypopigmented patches in Roberts/SC phocomelia syndrome occur via aneuploidy susceptibility. [科研必备] 专业SCI论文修改服务: 先修改后付款; 语言问题免费重修; 24-72小时交稿; 正规财务发票; 一分钟下单; 365日不间断服务 期刊全名 european journal of medical genetics 期刊简称 EUR J MED GENET. EUR J MED GENET 遗传学 医学 注:2010新增部分期刊未列入,目录分类来源于中国科学院,参考“期刊印证报告”(JCR),所收集信息仅供科学研究使用。 JCR 影响因子Impact factor, 5年期影响因子, 即年指数Immediacy ;. Year Bioxbio Journal Impact IF Total Articles Total Cites 2018/2019-2.197 343 11571 2017-2.264 399 11069 2016-2.259 403 10463 2015-2.082 416 9319 2014-2.159 435 9420 2013-2.048 414 8258 2012-2.304 421 7811 2011-2.391 399.

Eur J Med Genet 49:151–158 PubMed CrossRef Google Scholar 75. Borozdin W, Bravo Ferrer Acosta AM, Bramshad MJ et al 2006 Expanding the spectrum of TBX5 mutations in Holt-Oram syndrome: detection of two intragenic deletions by quantitative real time. Yeung A, Bruno D, Scheffer IE, Carranza D, Burgess T, Slater HR, Amor DJ. 4.45 Mb microduplication in chromosome band 14q12 including FOXG1 in a girl with refractory epilepsy and intellectual impairment. Eur J Med Genet.

BMC Medical Genetics is an open access journal publishing original peer-reviewed research articles in the effects of genetic variation in individuals, families and.

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