Author:
Ansseau Eugénie,Laoudj-Chenivesse Dalila,Marcowycz Aline,Tassin Alexandra,Vanderplanck Céline,Sauvage Sébastien,Barro Marietta,Mahieu Isabelle,Leroy Axelle,Leclercq India,Mainfroid Véronique,Figlewicz Denise,Mouly Vincent,Butler-Browne Gillian,Belayew Alexandra,Coppée Frédérique
Publisher
Public Library of Science (PLoS)
Reference60 articles.
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4. Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD) [published erratum appears in Hum Mol Genet 1995 Jul;4(7):1243-4].;PW Lunt;Hum Mol Genet,1995
5. Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotype.;E Ricci;Ann Neurol,1999
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