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No. ()
м (ȣ) Page ǿ ũ
10 Sihoun Hahn Molecular genetic testing of patients with monogenic diabetes and hyperinsulinism
Mol Genet Metab 114(3) 451-4 2015 pubmed
9 Sihoun Hahn() Novel mutations in ATP1A3 associated with catastrophic early life epilepsy, episodic prolonged apnea, and postnatal microcephaly
Epilepsia 56(3) 430 2015 pubmed
8 Sihoun Hahn() Utility of next generation sequencing in genetic diagnosis of early onset neuromuscular disorders
J Med Genet 52(3) 216 2015 pubmed
7 Sihoun Hahn() A Korean Case of -Ureidopropionase Deficiency Presenting with Intractable Seizure, Global Developmental Delay, and Microcephaly
JIMD Rep 19 121 2015 pubmed
6 Sung-Min Ahn Abstract A13: Establishment and characterization of patient-derived xenograft models of gastrointestinal stromal tumor resistant to standard tyrosine kinase inhibitors
Molecular Cancer Therapeutics 2015 pubmed

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