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European Journal of Human Genetics | mts-ejhg.nature.com Reviews
https://mts-ejhg.nature.com
eJournalPress is mission critical software providing online submission, review and tracking of manuscripts via the Internet. It was designed from the ground up to provide rock solid security, reliability and ease of use.
European Journal of Human Genetics
http://www.nature.com/ejhg/index.html
Jump to main content. Volume 24, No 9. 2015 Impact Factor 4.580*. 60/289 Biochemistry and Molecular Biology. 30/165 Genetics and Heredity. G-J B van Ommen. A maternal deletion upstream of the ICR2 in 11p15. Association of CAG in HTT with cancer prognosis. Structural implications of C1110S mutation in FLT1. Providers' view of online genetic counseling. GWAS of young–onset breast cancer. Current issue table of contents. Advance online publication in full. 2014 Journal Citation Reports. EU Cost Action BMI206.
European Journal of Human Genetics - Whole-genome sequencing in newborn screening[quest] A statement on the continued importance of targeted approaches in newborn screening programmes
http://www.nature.com/ejhg/journal/vaop/ncurrent/full/ejhg2014289a.html
Jump to main content. European Journal of Human Genetics. 1593–1600; doi:10.1038/ejhg.2014.289; published online 28 January 2015. Whole-genome sequencing in newborn screening ? A statement on the continued importance of targeted approaches in newborn screening programmes. Karine Sénécal. And endorsed by the European Society of Human Genetics; the P3G International Paediatric Platform; the Human Genome Organisation; and the PHG Foundation. Advance online publication 28 January 2015. It is foreseen that in...
European Journal of Human Genetics - Evolutionary Genetics: Is brain evolution still continuing in modern humans?
http://www.nature.com/ejhg/journal/v14/n7/full/5201624a.html
Jump to main content. European Journal of Human Genetics. 799–800. doi:10.1038/sj.ejhg.5201624; published online 29 March 2006. Evolutionary Genetics: Is brain evolution still continuing in modern humans? And Christopher Geoffrey Woods. Rowena Stern and Christopher G Woods are at the Department of Medical Genetics, Cambridge Institute of Medical Research, Addenbrooke's Hospital, Hills Road, Cambridge CB2 2XY, UK. Correspondence: Christopher Geoffrey Woods, E-mail: cw347@cam.ac.uk. Clues to the identities...
European Journal of Human Genetics - The X chromosome Alu insertions as a tool for human population genetics: data from European and African human groups
http://www.nature.com/ejhg/journal/v15/n5/full/5201797a.html
Jump to main content. European Journal of Human Genetics. 578–583. doi:10.1038/sj.ejhg.5201797; published online 28 February 2007. The X chromosome Alu insertions as a tool for human population genetics: data from European and African human groups. Unitat d'Antropologia, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain. Centre d'Anthropologie, University Toulouse III, Toulouse, France. Department of Biology, University of Crete, Herakleion, Greece. Alu repeats are a category of short inte...
origin.www.palgrave-journals.com
Submit your manuscript to npg : authors & referees @ npg
http://origin.www.palgrave-journals.com/authors/submit_manuscript.html
Jump to main content. If you would like to submit an article to one of the following journals, please click on the journal name below and you will be taken to the logon screen for the journal manuscript tracking system or the journals home page for specific instructions on how to submit a manuscript. American Journal of Gastroenterology. British Journal of Cancer. Cell Death and Differentiation. Cell Death and Disease. Cellular and Molecular Immunology. Clinical and Translational Gastroenterology. Nature...
European Journal of Human Genetics - Candidate genes for congenital diaphragmatic hernia from animal models: sequencing of FOG2 and PDGFR[alpha] reveals rare variants in diaphragmatic hernia patients
http://www.nature.com/ejhg/journal/v15/n9/full/5201872a.html
Jump to main content. European Journal of Human Genetics. 950–958; doi:10.1038/sj.ejhg.5201872; published online 13 June 2007. Candidate genes for congenital diaphragmatic hernia from animal models: sequencing of FOG2. Reveals rare variants in diaphragmatic hernia patients. And A M Slavotinek. Division of Medical Genetics, Department of Pediatrics, University of Utah, Salt Lake City, UT, USA. Division of Genetics, Department of Pediatrics, University of California, San Francisco, CA, USA. In a female wit...
European Journal of Human Genetics - Abstract of article: Transgenerational response to nutrition, early life circumstances and longevity
http://www.nature.com/ejhg/journal/v15/n7/abs/5201832a.html
Jump to main content. European Journal of Human Genetics. 784–790; doi:10.1038/sj.ejhg.5201832; published online 25 April 2007. Transgenerational response to nutrition, early life circumstances and longevity. And Michael Sjöström. Department of Public Health and Clinical Medicine, Umeå University, Umeå, Sweden. Department of Biosciences and Nutrition, Karolinska Institutet, Stockholm, Sweden. Department of Community Medicine and Rehabilitation, Umeå University, Umeå, Sweden. MORE ARTICLES LIKE THIS.
European Journal of Human Genetics - Prader-Willi syndrome
http://www.nature.com/ejhg/journal/v17/n1/full/ejhg2008165a.html
Jump to main content. European Journal of Human Genetics. 3–13; doi:10.1038/ejhg.2008.165; published online 10 September 2008. And Daniel J Driscoll. Division of Medical Genetics, Department of Pediatrics, University of California, San Francisco, CA, USA. Division of Genetics and Metabolism, Department of Pediatrics, University of Florida College of Medicine, Gainesville, FL, USA. Received 2 April 2008; Revised 15 July 2008; Accepted 17 July 2008; Published online 10 September 2008. Parental education ab...
European Journal of Human Genetics - Figure 1 for article: A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20//26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment
http://www.nature.com/ejhg/journal/v14/n10/fig_tab/5201670f1.html
Jump to main content. European Journal of Human Genetics. A novel missense mutation in ACTG1. Causes dominant deafness in a Norwegian DFNA20/26. Family, but ACTG1. Mutations are not frequent among families with hereditary hearing impairment. Nanna D Rendtorff, Mei Zhu, Toril Fagerheim, Torben L Antal, MaryPat Jones, Tanya M Teslovich, Elizabeth M Gillanders, Michael Barmada, Erik Teig, Jeffrey M Trent, Karen H Friderici, Dietrich A Stephan and Lisbeth Tranebjærg. Figure and tables index.
European Journal of Human Genetics - Ab initio prediction of mutation-induced cryptic splice-site activation and exon skipping
http://www.nature.com/ejhg/journal/v17/n6/full/ejhg2008257a.html
Jump to main content. European Journal of Human Genetics. 759–765; doi:10.1038/ejhg.2008.257; published online 14 January 2009. Prediction of mutation-induced cryptic splice-site activation and exon skipping. Division of Human Genetics, University of Southampton School of Medicine, Southampton, UK. Institute of Molecular Genetics, Czech Academy of Sciences, Prague, Czech Republic. International Centre for Genetic Engineering and Biotechnology, Trieste, Italy. Exon skipping, and the location and intrinsic...
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MTS Remote Services Bureau. CDMA, GSM And Microwave Networks. Hardware and Software Maintenance. In Business Since 1985. MTS has been diligently striving to provide unparalleled Value to our Clients through diversified range of progressive, proactive and cost effective solutions in virtually all aspects of the telecommunication guided by outstanding qualifications of staff and management, extensive on the job expertise, backed by dedication and integrity as the innate slogan of our company. SITA Airport ...
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European Journal of Clinical Nutrition
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European Journal of Human Genetics
Welcome to the European Journal of Human Genetics online manuscript submission and tracking system. The EJHG aims at international coverage of all aspects of human genetics; notably biochemical, clinical, cancer, molecular and population genetics, cytogenetics and molecular cytogenetics and genomics. Please be sure that you browser is set to accept cookies. Our tracking system requires them for proper operation. Experienced users please remember that passwords are case sensitive. Register for an account.
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