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Stem Cells (Dayton, Ohio)|February 3, 2015
Enhanced SMAD1 Signaling Contributes to Impairments of Early Development in CFC-iPSCsKyu-Min Han, Seung-Kyoon Kim, Dongkyu Kim, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 15, 2018
Biochemical and molecular analyses of infantile sialic acid storage disease in a patient with nonimmune hydrops fetalisEungu Kang, Yoon-Myung Kim, Sun Hee Heo, et al.
Journal of Human Genetics|May 22, 2015
Clinical outcomes and the mutation spectrum of the OTC gene in patients with ornithine transcarbamylase deficiencyJin-Ho Choi, Beom Hee Lee, Ja Hye Kim, et al.
BMC Medical Genomics|July 4, 2021
Ultra-rare renal diseases diagnosed with whole-exome sequencing: Utility in diagnosis and managementJiwon Jung, Joo Hoon Lee, Young Seo Park, et al.
Journal of Korean Medical Science|January 4, 2017
Genotype and Phenotype Analysis in Pediatric Patients with CystinuriaJi Hyun Kim, Eujin Park, Hye Sun Hyun, et al.
Journal of Korean Medical Science|February 6, 2009
Two Korean infants with genetically confirmed congenital nephrotic syndrome of Finnish typeBeom Hee Lee, Yo Han Ahn, Hyun Jin Choi, et al.
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