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Publications by Pascaline Gaildrat

Identification of Variants in the 4q35 GeneFAT1in Patients With a Facioscapulohumeral Dystrophy-Like Phenotype

English

Detecting Splicing Patterns in Genes Involved in Hereditary Breast and Ovarian Cancer

European Journal of Human Genetics

English

Related publications

Identification of Variants in MBNL1 in Patients With a Myotonic Dystrophy-Like Phenotype

European Journal of Human Genetics

English

Facioscapulohumeral Muscular Dystrophy

English

Facioscapulohumeral Muscular Dystrophy

Current Neurology and Neuroscience Reports

English

Thoracoscapular Fusion for Facioscapulohumeral Dystrophy

The Journal of Bone and Joint Surgery. British volume

English

Electrical Impedance Myography in Facioscapulohumeral Muscular Dystrophy

Muscle and Nerve

Molecular Neuroscience

English

Distinguishing the 4qA and 4qB Variants Is Essential for the Diagnosis of Facioscapulohumeral Muscular Dystrophy in the Chinese Population

European Journal of Human Genetics

English

The Long and Short of Facioscapulohumeral Muscular Dystrophy

English

Elderly Onset of Weakness in Facioscapulohumeral Muscular Dystrophy

Case Reports in Neurological Medicine

English

An RCS-Like Retinal Dystrophy Phenotype inMerKnockout Mice

Investigative Ophthalmology and Visual Science

Molecular Neuroscience

Sensory Systems

English