Found: 7
Select item for more details and to access through your institution.
Interpretation of the Epigenetic Signature of Facioscapulohumeral Muscular Dystrophy in Light of Genotype-Phenotype Studies.
- Published in:
- International Journal of Molecular Sciences, 2020, v. 21, n. 7, p. 2635, doi. 10.3390/ijms21072635
- By:
- Publication type:
- Article
Large scale genotype-phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophy.
- Published in:
- 2013
- By:
- Publication type:
- journal article
Large scale genotype–phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophy.
- Published in:
- Brain: A Journal of Neurology, 2013, v. 136, n. 11, p. 3408, doi. 10.1093/brain/awt226
- By:
- Publication type:
- Article
Phenotypic Variability Among Patients With D4Z4 Reduced Allele Facioscapulohumeral Muscular Dystrophy.
- Published in:
- JAMA Network Open, 2020, v. 3, n. 5, p. e204040, doi. 10.1001/jamanetworkopen.2020.4040
- By:
- Publication type:
- Article
A 5-year clinical follow-up study from the Italian National Registry for FSHD.
- Published in:
- Journal of Neurology, 2021, v. 268, n. 1, p. 356, doi. 10.1007/s00415-020-10144-7
- By:
- Publication type:
- Article
A novel clinical tool to classify facioscapulohumeral muscular dystrophy phenotypes.
- Published in:
- Journal of Neurology, 2016, v. 263, n. 6, p. 1204, doi. 10.1007/s00415-016-8123-2
- By:
- Publication type:
- Article
Large genotype–phenotype study in carriers of D4Z4 borderline alleles provides guidance for facioscapulohumeral muscular dystrophy diagnosis.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-78578-7
- By:
- Publication type:
- Article