TY  - GEN
AU  - Pikó,Henriett
AU  - Molnár,Mária Judit
AU  - Herczegfalvi,Agnes
AU  - Mayer,Péter
AU  - Karcagi,Veronika
TI  - [Role of associated alleles and hypomethylation status in the clinical expression of facioscapulohumeral muscular dystrophy]
SN  - 0030-6002
PY  - 2011///1114
KW  - Alleles
KW  - Blotting, Southern
KW  - Chromosomes, Human, Pair 4
KW  - genetics
KW  - DNA Methylation
KW  - Epigenesis, Genetic
KW  - Humans
KW  - Muscular Dystrophy, Facioscapulohumeral
KW  - Phenotype
KW  - Repetitive Sequences, Nucleic Acid
KW  - Telomere
N1  - Publication Type: English Abstract; Journal Article
UR  - https://doi.org/10.1556/OH.2011.29179
ER  -