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Recommendations for the predictive genetic test in Huntington's disease.

MacLeod R, Tibben A, Frontali M, Evers-Kiebooms G, Jones A, Martinez-Descales A, Roos RA; Editorial Committee and Working Group ‘Genetic Testing Counselling’ of the European Huntington Disease Network.

Clin Genet. 2013 Mar;83(3):221-31. doi: 10.1111/j.1399-0004.2012.01900.x. Epub 2012 Jul 30. No abstract available.


Fragile XE: an important differential diagnosis.

Krishnan V, Clouston P, Crocker M, Macpherson J, Heydon F, Stewart H.

BMJ Case Rep. 2010;2010. pii: bcr06.2009.1964. doi: 10.1136/bcr.06.2009.1964. Epub 2010 Mar 23.


Reduced penetrance alleles for Huntington's disease: a multi-centre direct observational study.

Quarrell OW, Rigby AS, Barron L, Crow Y, Dalton A, Dennis N, Fryer AE, Heydon F, Kinning E, Lashwood A, Losekoot M, Margerison L, McDonnell S, Morrison PJ, Norman A, Peterson M, Raymond FL, Simpson S, Thompson E, Warner J.

J Med Genet. 2007 Mar;44(3):e68.

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