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Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics.
Carrieri D, Howard HC, Benjamin C, Clarke AJ, Dheensa S, Doheny S, Hawkins N, Halbersma-Konings TF, Jackson L, Kayserili H, Kelly SE, Lucassen AM, Mendes Á, Rial-Sebbag E, Stefánsdóttir V, Turnpenny PD, van El CG, van Langen IM, Cornel MC, Forzano F; European Society of Human Genetics. Carrieri D, et al. Among authors: van el cg, van langen im. Eur J Hum Genet. 2019 Feb;27(2):169-182. doi: 10.1038/s41431-018-0285-1. Epub 2018 Oct 11. Eur J Hum Genet. 2019. PMID: 30310124 Free PMC article.
Italian appeal court: a genetic predisposition to commit murder?
Forzano F, Borry P, Cambon-Thomsen A, Hodgson SV, Tibben A, de Vries P, van El C, Cornel M. Forzano F, et al. Eur J Hum Genet. 2010 May;18(5):519-21. doi: 10.1038/ejhg.2010.31. Epub 2010 Mar 10. Eur J Hum Genet. 2010. PMID: 20216573 Free PMC article.
Genetic testing and common disorders in a public health framework.
van El CG, Cornel MC; ESHG Public and Professional Policy Committee. van El CG, et al. Eur J Hum Genet. 2011 Apr;19(4):377-81. doi: 10.1038/ejhg.2010.176. Epub 2011 Jan 26. Eur J Hum Genet. 2011. PMID: 21267009 Free PMC article. No abstract available.
Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities. Background Document to the ESHG recommendations on genetic testing and common disorders.
Becker F, van El CG, Ibarreta D, Zika E, Hogarth S, Borry P, Cambon-Thomsen A, Cassiman JJ, Evers-Kiebooms G, Hodgson S, Janssens AC, Kaariainen H, Krawczak M, Kristoffersson U, Lubinski J, Patch C, Penchaszadeh VB, Read A, Rogowski W, Sequeiros J, Tranebjaerg L, van Langen IM, Wallace H, Zimmern R, Schmidtke J, Cornel MC. Becker F, et al. Among authors: van el cg, van langen im. Eur J Hum Genet. 2011 Apr;19 Suppl 1(Suppl 1):S6-44. doi: 10.1038/ejhg.2010.249. Eur J Hum Genet. 2011. PMID: 21412252 Free PMC article. Review. No abstract available.
Public support for neonatal screening for Pompe disease, a broad-phenotype condition.
Weinreich SS, Rigter T, van El CG, Dondorp WJ, Kostense PJ, van der Ploeg AT, Reuser AJ, Cornel MC, Hagemans ML. Weinreich SS, et al. Among authors: van der ploeg at, van el cg. Orphanet J Rare Dis. 2012 Mar 14;7:15. doi: 10.1186/1750-1172-7-15. Orphanet J Rare Dis. 2012. PMID: 22413814 Free PMC article.
The changing landscape of genetic testing and its impact on clinical and laboratory services and research in Europe.
Hastings R, de Wert G, Fowler B, Krawczak M, Vermeulen E, Bakker E, Borry P, Dondorp W, Nijsingh N, Barton D, Schmidtke J, van El CG, Vermeesch J, Stol Y, Carmen Howard H, Cornel MC. Hastings R, et al. Among authors: van el cg. Eur J Hum Genet. 2012 Sep;20(9):911-6. doi: 10.1038/ejhg.2012.56. Epub 2012 Mar 28. Eur J Hum Genet. 2012. PMID: 22453292 Free PMC article.
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