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Results: 10

Cited In for PubMed (Select 17873651)


Clinical impact of copy number variation analysis using high-resolution microarray technologies: advantages, limitations and concerns.

Coughlin CR 2nd, Scharer GH, Shaikh TH.

Genome Med. 2012 Oct 30;4(10):80. doi: 10.1186/gm381. eCollection 2012. Review.


Ethical issues in neonatal and pediatric clinical trials.

Laventhal N, Tarini BA, Lantos J.

Pediatr Clin North Am. 2012 Oct;59(5):1205-20. doi: 10.1016/j.pcl.2012.07.007. Epub 2012 Aug 26. Review.


To tell or not to tell? A systematic review of ethical reflections on incidental findings arising in genetics contexts.

Christenhusz GM, Devriendt K, Dierickx K.

Eur J Hum Genet. 2013 Mar;21(3):248-55. doi: 10.1038/ejhg.2012.130. Epub 2012 Jun 27. Review.


"What does it mean?": uncertainties in understanding results of chromosomal microarray testing.

Reiff M, Bernhardt BA, Mulchandani S, Soucier D, Cornell D, Pyeritz RE, Spinner NB.

Genet Med. 2012 Feb;14(2):250-8. doi: 10.1038/gim.2011.52. Epub 2012 Jan 5.


Social Responsiveness Scale-aided analysis of the clinical impact of copy number variations in autism.

van Daalen E, Kemner C, Verbeek NE, van der Zwaag B, Dijkhuizen T, Rump P, Houben R, van 't Slot R, de Jonge MV, Staal WG, Beemer FA, Vorstman JA, Burbach JP, van Amstel HK, Hochstenbach R, Brilstra EH, Poot M.

Neurogenetics. 2011 Nov;12(4):315-23. doi: 10.1007/s10048-011-0297-2. Epub 2011 Aug 12.


Practical guidelines addressing ethical issues pertaining to the curation of human locus-specific variation databases (LSDBs).

Povey S, Al Aqeel AI, Cambon-Thomsen A, Dalgleish R, den Dunnen JT, Firth HV, Greenblatt MS, Barash CI, Parker M, Patrinos GP, Savige J, Sobrido MJ, Winship I, Cotton RG; Ethics Committee of the Human Genome Organization (HUGO).

Hum Mutat. 2010 Nov;31(11):1179-84. doi: 10.1002/humu.21339.


What is a meaningful result? Disclosing the results of genomic research in autism to research participants.

Miller FA, Hayeems RZ, Bytautas JP.

Eur J Hum Genet. 2010 Aug;18(8):867-71. doi: 10.1038/ejhg.2010.34. Epub 2010 Mar 17.


Translating genomics into the clinic: moving to the post-Mendelian world.

Cho MK.

Genome Med. 2009 Jan 20;1(1):7. doi: 10.1186/gm7.


Understanding incidental findings in the context of genetics and genomics.

Cho MK.

J Law Med Ethics. 2008 Summer;36(2):280-5, 212. doi: 10.1111/j.1748-720X.2008.00270.x.


Ethical and social implications of genetic testing for communication disorders.

Arnos KS.

J Commun Disord. 2008 Sep-Oct;41(5):444-57. doi: 10.1016/j.jcomdis.2008.03.001. Epub 2008 Mar 25. Review.

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