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History (55)
De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome.
Memories of the McNutt fellowship.
Novel mutations in ATP1A3 associated with catastrophic early life epilepsy, episodic prolonged apnea, and postnatal microcephaly.
Pharmacodynamics of fluorouracil-based induction chemotherapy in advanced head and neck cancer.
Detection of facial hypotonia and diagnosis of facioscapulohumeral dystrophy.
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Detection of facial hypotonia and diagnosis of facioscapulohumeral dystrophy.
Detection of facial hypotonia and diagnosis of facioscapulohumeral dystrophy. Arch Ophthalmol. 2008 May; 126(5):745-6; author reply 746.
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subject areas
Chromosome Deletion
Chromosomes, Human, Pair 4
Eye Enucleation
Facial Muscles
Fluorescein Angiography
Glaucoma, Neovascular
Humans
Intraocular Pressure
Laser Coagulation
Muscle Hypotonia
Muscular Dystrophy, Facioscapulohumeral
Retinal Diseases
Retinal Vessels
Telangiectasis
authors with profiles
Veeral Sheth