@article {6726,
	title = {EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH)},
	journal = {European Journal of Human Genetics},
	volume = {24},
	year = {2016},
	note = {Cited By :14Export Date: 19 March 2018},
	month = {2016},
	pages = {479 - 495},
	url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-84960397668\&doi=10.1038\%2fejhg.2015.128\&partnerID=40\&md5=aedb529de1d8bca3adccfd3b56da9190},
	author = {Porto, G. and Brissot, P. and Swinkels, D.W. and Zoller, H. and Kamarainen, O. and Patton, S. and Alonso, I. and Morris, M. and Keeney, S.}
}
@booklet {5407,
	title = {EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH)},
	howpublished = {European Journal of Human Genetics},
	year = {2015},
	note = {Export Date: 12 January 2016Article in Press},
	month = {2015},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84936976676\&partnerID=40\&md5=3615d95c94f3beac334811fe5e75251d},
	author = {Porto, G. and Brissot, P. and Swinkels, D.W. and Zoller, H. and Kamarainen, O. and Patton, S. and Alonso, I. and Morris, M. and Keeney, S.}
}
@article {3656,
	title = {Experience and outcome of 3 years of a European EQA scheme for genetic testing of the spinocerebellar ataxias},
	journal = {European Journal of Human Genetics},
	volume = {16},
	year = {2008},
	note = {Cited By (since 1996): 12Export Date: 18 March 2013Source: Scopus},
	month = {2008///},
	pages = {913 - 920},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-48249128741\&partnerID=40\&md5=73d2af57021a502c6a58c54c79e96732},
	author = {Seneca, S. and Morris, M.A. and Patton, S. and Elles, R. and Sequeiros, J.}
}
