Detalhe da pesquisa
1.
Next Generation Sequencing is a Reliable Tool for Detecting BRCA1/2 Mutations, Including Large Genomic Rearrangements.
Clin Lab
; 68(2)2022 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35142179
2.
Severe Acute Respiratory Syndrome Coronavirus-2 Antibody Responses in Hospitalized Patients with Coronavirus Disease 2019 in Daegu, Korea.
Clin Lab
; 67(11)2021 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34758229
3.
Autoimmune cytopenia in a Korean pediatric patient with Kabuki syndrome treated with sirolimus.
Pediatr Blood Cancer
; 70(6): e30275, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36860120
4.
A case of inherited type 1 and type 2A von Willebrand disease confirmed by diagnostic exome sequencing.
Pediatr Blood Cancer
; 65(10): e27279, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29893454
5.
Comparison of the Automated cobas u 701 Urine Microscopy and UF-1000i Flow Cytometry Systems and Manual Microscopy in the Examination of Urine Sediments.
J Clin Lab Anal
; 30(5): 663-71, 2016 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26842372
6.
Sequential strategy for umbilical cord blood transplantation in a Korean Fanconi anemia girl with refractory acute myelomonocytic leukemia and complex karyotype.
Pediatr Transplant
; 21(2)2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-27976485
7.
Subpopulations of regulatory T cells in rheumatoid arthritis, systemic lupus erythematosus, and Behcet's disease.
J Korean Med Sci
; 27(9): 1009-13, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22969245
8.
The Effect of NUDT15, TPMT, APEX1, and ITPA Genetic Variations on Mercaptopurine Treatment of Pediatric Acute Lymphoblastic Leukemia.
Children (Basel)
; 8(3)2021 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33804051
9.
Diagnosis of Duchenne Muscular Dystrophy in a Presymptomatic Infant Using Next-Generation Sequencing and Chromosomal Microarray Analysis: A Case Report.
Children (Basel)
; 8(5)2021 May 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34064562
10.
A Population-Based Analysis of BRCA1/2 Genes and Associated Breast and Ovarian Cancer Risk in Korean Patients: A Multicenter Cohort Study.
Cancers (Basel)
; 13(9)2021 May 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34063308
11.
Genetic Confirmation and Identification of Novel Variants for Glanzmann Thrombasthenia and Other Inherited Platelet Function Disorders: A Study by the Korean Pediatric Hematology Oncology Group (KPHOG).
Genes (Basel)
; 12(5)2021 05 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34066320
12.
An optimized BRCA1/2 next-generation sequencing for different clinical sample types.
J Gynecol Oncol
; 31(1): e9, 2020 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-31788999
13.
BRCA1/2 mutations, including large genomic rearrangements, among unselected ovarian cancer patients in Korea.
J Gynecol Oncol
; 29(6): e90, 2018 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-30207098
14.
The first Korean case with Floating-Harbor syndrome with a novel SRCAP mutation diagnosed by targeted exome sequencing.
Korean J Pediatr
; 61(12): 403-406, 2018 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-30304910
15.
Three Cases of False-positive Multiplex Ligation-dependent Probe Amplification of BRCA1.
Ann Lab Med
; 42(4): 497-499, 2022 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35177575
16.
Possible new LNK mutations in myeloproliferative neoplasms.
Am J Hematol
; 86(10): 866-8, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21922527
17.
Up-regulation of MicroRNA 146b is Associated with Myelofibrosis in Myeloproliferative Neoplasms.
Ann Clin Lab Sci
; 45(3): 308-14, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26116595
18.
Calreticulin exon 9 mutations in myeloproliferative neoplasms.
Ann Lab Med
; 35(1): 22-7, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25553276
19.
Thrombocythemia 1 With THPO Variant (c.13+1G>A) Diagnosed Using Targeted Exome Sequencing: First Case in Korea.
Ann Lab Med
; 40(4): 341-344, 2020 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-32067437
20.
Prenatal diagnosis of a 7q21.13q22.1 deletion detected using high-resolution microarray.
Obstet Gynecol Sci
; 57(4): 318-24, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25105107