Browsing by Keyword : Karyotyping
Showing results 1 to 13 of 13
| Pub Year | | Title | AJOU Author(s) |
| 2011 | | Acquisition of a BCR-ABL1 transcript in a patient with disease progression from MDS with fibrosis to AML with myelodysplasia-related changes. | 김현주, 김효철, 박준성, 이현우, 정성현, 조성란 |
| 2010 | | Acute myeloid leukemia with t(16;21)(q24;q22) and eosinophilia: case report and review of the literature. | 김현주, 박일중, 박준은, 이위교, 조성란 |
| 2022 | | Chromosomal abnormalities of 19,000 couples with recurrent spontaneous abortions: a multicenter study | 박서진 |
| 2013 | | Clinical and cytogenetic features of a patient with partial trisomy 8q and partial monosomy 13q delineated by array comparative genomic hybridization. | 김성환, 박문성, 손영배, 이장훈 |
| 2010 | | Clinical features and outcomes of holoprosencephaly in Korea. | 고정민, 김성환 |
| 2015 | | Diagnostic approach for genetic causes of intellectual disability. | 임신영 |
| 2012 | | Familial Xp22.33-Xp22.12 deletion delineated by chromosomal microarray analysis causes proportionate short stature | 손영배 |
| 2002 | | Immortalization of rat eustachian tube epithelial cells by adenovirus 12-simian virus 40 hybrid virus. | 문성균 |
| 2010 | | Influence of parental origin of the X chromosome on physical phenotypes and GH responsiveness of patients with Turner syndrome. | 고정민 |
| 1996 | | MLL tandem duplication and multiple splicing in adult acute myeloid leukemia with normal karyotype. | 남동기 |
| 2010 | | Molecular cytogenetic analysis of Korean patients with Waldenström macroglobulinemia. | 조성란 |
| 2010 | | Partial tetrasomy of chromosome 22q11.1 resulting from a supernumerary isodicentric marker chromosome in a boy with cat-eye syndrome. | 고정민, 배기수 |
| 2010 | | The common exon 3 polymorphism of the growth hormone receptor gene and the effect of growth hormone therapy on growth in Korean patients with Turner syndrome. | 고정민 |
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