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Keyword [D4Z4]
Result: 1 - 7 | Page: 1 of 1
1.
Study On The Molecular Genetics And Gene Diagnosis Of Facioscapulohumeral Muscular Dystrophy In Chinese
2.
Establishment Of Pulsed Field Gel Electrophoresis System And Study On The Gene Structure Of Facioscapulohumeral Muscular Dystrophy In Chinese Population
3.
Analysis Of The Genetic Characterization Of SSLP-D4Z4-4qA/qB-PLAM In Patients With FSAM And Its Association With Clinical Phenotype In Chinese Han Population
4.
Correlation Between D4Z4 Repeats And Phenotype In Facioscapulohumeral Muscular Dystrophy
5.
Association Of Phenotype-Genotype And Methylation In 4q35-D4Z4/PAS Region Of FSHD
6.
Transcriptional profiles in facioscapulohumeral muscular dystrophy and possible disease mechanisms
7.
DNA methylation and constitutive heterochromatin in the ICF syndrome, FSHD syndrome, and normal human embryonic cell cultures
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