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Showing results 1 to 9 of 9

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Issue Date	Title	Journal Title
2007	A der(1;15)(q10;q10) is a rare nonrandom whole-arm translocation in patients with acute lymphoblastic leukemia	CANCER GENETICS AND CYTOGENETICS
2018	A New Integrated Newborn Screening Workflow Can Provide a Shortcut to Differential Diagnosis and Confirmation of Inherited Metabolic Diseases	YONSEI MEDICAL JOURNAL
2013	A novel F11 mutation in a Korean pediatric patient with recurrent epistaxis	BLOOD COAGULATION & FIBRINOLYSIS
2010	An SRY-deleted XXY female resulting from a paternally inherited t(Y;22)	ANNALS OF CLINICAL AND LABORATORY SCIENCE
2009	BCR/ABL rearrangement with b3a3 fusion transcript in a case of childhood acute lymphoblastic leukemia.	CANCER GENETICS AND CYTOGENETICS
2009	De novo interstitial direct duplication 8 (p21.3p23.1) with Pierre Robin sequence	Korean Journal of Pediatrics
2016	Diagnosis of Severe Protein C Deficiency Confirmed by Presence of Rare PROC Gene Mutation	Neonatal Medicine
2012	Population-specific spectrum of the F11 mutations in Koreans: evidence for a founder effect.	CLINICAL GENETICS
2010	Three-way translocation involving MLL, MLLT1, and a novel third partner, NRXN1, in a patient with acute lymphoblastic leukemia and t(2;19;11) (p12;p13.3;q23).	CANCER GENETICS AND CYTOGENETICS