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Keyword [FSHD]
Result: 1 - 13 | Page: 1 of 1
1.
Genetic Research Of 4q35 In Facioscapulohumeral Muscular Dystrophy(FSHD)
2.
The Clinical And Histopathological Features Of Facioscapulohumeral Muscular Dystrophy (FSHD) And The Study Of Vascular Factors In The Pathogenesis Of FSHD
3.
Study On The Molecular Genetics And Gene Diagnosis Of Facioscapulohumeral Muscular Dystrophy In Chinese
4.
Establishment Of Pulsed Field Gel Electrophoresis System And Study On The Gene Structure Of Facioscapulohumeral Muscular Dystrophy In Chinese Population
5.
Facioscapulohumeral Muscular Dystrophy In Chinese Population Characteristics Of Alleles 4qA/4qB In 4q Subtelomere
6.
Mutation Spectrum And Phenotypic Manifestation In FSHD Chinese Patients
7.
Structural And Functional Study Of Oncoprotein DUX4/IGH In Acute B Lymphoblastic Leukemia
8.
Association Of Phenotype-Genotype And Methylation In 4q35-D4Z4/PAS Region Of FSHD
9.
Altered FRG1 levels during Xenopus laevis development leads to muscular and vascular phenotypes supporting a role for the misregulation of FRG1 in FSHD
10.
Transcriptional profiles in facioscapulohumeral muscular dystrophy and possible disease mechanisms
11.
Gene Therapy for Facioscapulohumeral Muscular Dystrophy
12.
DNA methylation and constitutive heterochromatin in the ICF syndrome, FSHD syndrome, and normal human embryonic cell cultures
13.
The Phenotype-genotype Analysis Of Wheelchair-dependent Patients With FSHD As Well As Preliminary Study In A FSHD Mouse Model Of DUX4-cre
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