Publications by authors named "Nollaig A Parfrey"

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Homozygous SLC4A11 mutation in a large Irish CHED2 pedigree.
Collette K Hand, Mairide McGuire, Nollaig A Parfrey, Conor C Murphy

Ophthalmic Genet· November 2017

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Phenotypic Variation in a Caucasian Kindred with Chorea-Acanthocytosis.
Áine Merwick, Tzehow Mok, Brian McNamara, Nollaig A Parfrey, Helena Moore

Mov Disord Clin Pract· March 2015

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A novel locus for restless legs syndrome maps to chromosome 19p in an Irish pedigree.
Evelyn B Skehan, Manal M A Abdulrahim, Nollaig A Parfrey, Collette K Hand

Neurogenetics· May 2012

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A novel ATP1A2 gene mutation in an Irish familial hemiplegic migraine kindred.
Desiree M Fernandez, Collette K Hand, Brian J Sweeney, Nollaig A Parfrey

Headache· January 2008

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Association of NOD2 with Crohn's disease in a homogenous Irish population.
Emer Bairead, Dawn L Harmon, Anne M Curtis, Yvette Kelly, Clare O'Leary, Nollaig A Parfrey

Eur J Hum Genet· March 2003

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