MOLECULARGENETICS-AssociationforClinicalGenetic…:分子遗传学-临床遗传协会….docxVIP

MOLECULARGENETICS-AssociationforClinicalGenetic…:分子遗传学-临床遗传协会….docx

  1. 1、原创力文档(book118)网站文档一经付费(服务费),不意味着购买了该文档的版权,仅供个人/单位学习、研究之用,不得用于商业用途,未经授权,严禁复制、发行、汇编、翻译或者网络传播等,侵权必究。。
  2. 2、本站所有内容均由合作方或网友上传,本站不对文档的完整性、权威性及其观点立场正确性做任何保证或承诺!文档内容仅供研究参考,付费前请自行鉴别。如您付费,意味着您自己接受本站规则且自行承担风险,本站不退款、不进行额外附加服务;查看《如何避免下载的几个坑》。如果您已付费下载过本站文档,您可以点击 这里二次下载
  3. 3、如文档侵犯商业秘密、侵犯著作权、侵犯人身权等,请点击“版权申诉”(推荐),也可以打举报电话:400-050-0827(电话支持时间:9:00-18:30)。
  4. 4、该文档为VIP文档,如果想要下载,成为VIP会员后,下载免费。
  5. 5、成为VIP后,下载本文档将扣除1次下载权益。下载后,不支持退款、换文档。如有疑问请联系我们
  6. 6、成为VIP后,您将拥有八大权益,权益包括:VIP文档下载权益、阅读免打扰、文档格式转换、高级专利检索、专属身份标志、高级客服、多端互通、版权登记。
  7. 7、VIP文档为合作方或网友上传,每下载1次, 网站将根据用户上传文档的质量评分、类型等,对文档贡献者给予高额补贴、流量扶持。如果你也想贡献VIP文档。上传文档
查看更多
MOLECULARGENETICS-AssociationforClinicalGenetic…:分子遗传学-临床遗传协会….docx

Participants Meeting 2014Thursday 15th May 201410:30am - 3:30pmKennedy Lecture Theatre, Institute of Child Health, 30 Guildford Street, London, UKRegistration formYou are invited to the UK NEQAS for Molecular Genetics participants meeting 2014 which will be focussing on the two key issues arising from the 2013 EQA scheme. The morning sessions will cover Human Genetic Variation Society mutation nomenclature guidelines giving laboratories an opportunity to submit queries prior to the meeting and obtain feedback from the HGVS committee. The afternoon sessions will comprise of interpretation of sequence variants and in particular potential splicing mutations.There will be no attendance fee and refreshments and lunch will be provided. Attendance will be based on a first come first served basis and limited to two individuals from each laboratory. Registration closes at the end of Wednesday 7th May, 2014.Name:Laboratory:Postal address:Telephone number:Email address:If you have any special dietary requirements or disabilities then please give details:Please tick the relevant box below and the Scheme will contact you directly at the email address supplied above. Please note that due to time constraints we may not be able to discuss all queries.I would like to submit a HGVS mutation nomenclature query: I would like to submit a sequence variant query:Please return your completed form to:Dr Sandi Deans, UK NEQAS for Molecular Genetics, Department of Laboratory Medicine, The Royal Infirmary of Edinburgh, 51 Little France Crescent, Edinburgh EH16 4SA, United KingdomEmail: Sandi.Deans@ed.ac.uk / Fax: +44 (0)131 242 6898If you have any queries then please do not hesitate to contact the Scheme at mailto:info@.ukinfo@.ukKind Regards,Dr Sandi Deans Scheme DirectorUK NEQAS for Molecular GeneticsUK NEQAS for Molecular Pathology UK NEQAS for Molecular Genetics .uk Director: Dr Sandi Deans Scheme email: info@.uk Scheme telephone: +44 (0) 131 242 6898Scheme fax: +44 (0) 131 242 6882UK N

文档评论(0)

docindoc + 关注
实名认证
文档贡献者

该用户很懒,什么也没介绍

1亿VIP精品文档

相关文档