Related content

The Evolutionary Distribution and Structural Organization of the Homeobox-Containing Repeat D4Z4 Indicates a Functional Role for the Ancestral Copy in the FSHD Region

By Winokur Sara T.   Bengtsson Ulla   Vargas Julie C.   Wasmuth John J.   Altherr Michael R.  

Human Molecular Genetics, Vol. 5, Iss. 10, 1996-10 ,pp. : 1567-1575

Oxford University Press

Access to resources Recommend Favorite

Localization of 4q35.2 to the nuclear periphery: is FSHD a nuclear envelope disease?

By Masny Peter S.  

Human Molecular Genetics, Vol. 13, Iss. 17, 2004-09 ,pp. : 1857-1871

Oxford University Press

Access to resources Recommend Favorite

Inter- and intrachromosomal sub-telomeric rearrangements on 4q35: implications for facioscapulohumeral muscular dystrophy (FSHD) aetiology and diagnosis

By Padberg G.W.  

Human Molecular Genetics, Vol. 7, Iss. 8, 1998-08 ,pp. : 1207-1214

Oxford University Press

Access to resources Recommend Favorite

Identification of the First Gene ( FRG1 ) from the FSHD Region on Human Chromosome 4q35

By van Deutekom Judith C. T.   Lemmers Richard J. L. F.   Grewal Prabhjit K.   van Geel Michel   Romberg Silke   Dauwerse Hans G.   Wright Tracy J.   Padberg George W.   Hofker Marten H.   Hewitt Jane E.   Frants Rune R.  

Human Molecular Genetics, Vol. 5, Iss. 5, 1996-01 ,pp. : 581-590

Oxford University Press

Access to resources Recommend Favorite

Antisense Oligonucleotides Used to Target the DUX4 mRNA as Therapeutic Approaches in FaciosScapuloHumeral Muscular Dystrophy (FSHD)

By Ansseau Eugénie   Vanderplanck Céline   Wauters Armelle   Harper Scott Q.   Coppée Frédérique   Belayew Alexandra  

Genes, Vol. 8, Iss. 3, 2017-03 ,pp. : 93-93

MDPI

Access to resources Recommend Favorite