Kok, Fernando
Resultados: Listando 10 de 18 en la página 1 de 2
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Nerve conduction studies on SPOAN syndrome
Whole exome sequencing in the diagnosis of cerebellar developmental and brain neuronal...
The ancestry of Brazilian Northeast populations with high frequency of consanguineous...
Hypomyelination: clinical, electrophysiological, and neuroimaging characterizati...
Clinical and genetic investigation of hereditary spastic paraplegia
Functional and motor characterization of spastic paraplegia, optic atrophy and peripheral...
Contribution to clinical characterization of autosomal recessive hereditary atax...
Biochemical diagnosis of creatine deficiency syndromes
Investigation of chromosomal abnormalities in patients with corpus callosum malf...
Unraveling the molecular basis of SPOAN syndrome: deletion in homozygosis inregulatory...
Resultados: Listando 10 de 18 en la página 1 de 2
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