HuGE Literature Finder
Records 1 - 2
| A Wide Spectrum of Genetic Disorders Causing Severe Childhood Epilepsy in Taiwan: A Case Series of Ultrarare Genetic Cause and Novel Mutation Analysis in a Pilot Study.
Journal of personalized medicine 2020 12 10 (4): .
Hong Syuan-Yu, Yang Jiann-Jou, Li Shuan-Yow, Lee Inn-C
| Genotype-phenotype correlation of Coffin-Siris syndrome caused by mutations in SMARCB1, SMARCA4, SMARCE1, and ARID1A.
American journal of medical genetics. Part C, Seminars in medical genetics 2014 Sep 166C (3): 262-75.
Kosho Tomoki, Okamoto Nobuhiko,
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