Showing results 14 to 16 of 16
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Title | Author(s) | Issue Date | Views | |
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Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome. Journal:Journal of medical genetics | 2000 | 146 | ||
Two novel CLN2 gene mutations in an Chinese patient with classical late-infantile neuronal ceroid lipofuscinosis [2] Journal:American Journal of Medical Genetics | 2001 | 183 | ||
2021 | 23 |