Showing results 11 to 16 of 16
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Title | Author(s) | Issue Date | Views | |
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De novo mutation in the mitochondrial tRNALeu(UUR) gene (A3243G) with rapid segregation resulting in MELAS in the offspring Journal:Journal of Paediatrics and Child Health | 2001 | 179 | ||
2011 | 206 | |||
Randomised control trial of tongue acupuncture versus sham acupuncture in improving functional outcome in cerebral palsy Journal:Journal of Neurology, Neurosurgery and Psychiatry | 2004 | |||
Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome. Journal:Journal of medical genetics | 2000 | 169 | ||
Two novel CLN2 gene mutations in an Chinese patient with classical late-infantile neuronal ceroid lipofuscinosis [2] Journal:American Journal of Medical Genetics | 2001 | 199 | ||
2021 | 23 |