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Chromosomal Abnormalities in Korean Fetuses with Nuchal Translucency above the 99th Percentile

Kwak DW, Boo H, Chang EH, Ryu HM, Han YJ, Chung JH, Kim MY, Yang EJ, Yoo HJ, Kim JW

OBJECTIVE: To evaluate the prevalence and distribution of chromosomal defects in Korean fetuses with nuchal translucency (NT) above the 99th percentile and to analyze them according to the degree of...
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Clinicopathological features of premature ovarian insufficiency associated with chromosome abnormalities

Jo HC, Park JK, Baek JC, Park JE, Kang MY, Cho IA

PURPOSE: The aim of this study was to investigate the clinicopathological features of premature ovarian insufficiency (POI) associated with chromosomal abnormalities. MATERIALS AND METHODS: This was a retrospective study of POI...
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Genetic Screening for Chromosomal Abnormalities and Y Chromosome Microdeletions in 846 Infertile Korean Men

Han SH, Bak CW, Cho H, Ban GW, Kang JS, Lim HS, Lee KR, Hwang SY

BACKGROUND: Chromosomal abnormalities are confirmed as one of the frequent causes of male infertility. The microdeletion of the azoospermia factor (AZF) region in the Y chromosome was discovered as another...
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Change in rates of prenatal tests for chromosomal abnormality over a 12-year period in women of advanced maternal age

Kim SM, Kim HH, Han YJ, Choi JS, Ryu HM, Yang S, Kim MH

OBJECTIVE: In 2007, the American College of Obstetricians and Gynecologists (ACOG) recommended that all pregnant women be offered screening or diagnostic tests for chromosomal abnormalities regardless of their age. Noninvasive...
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Additional cytogenetic aberrations in chronic myeloid leukemia: a single-center experience in the Middle East

Safaei A, Monabati A, Safavi M, Atashabparvar A, Hosseini M

BACKGROUND: Additional cytogenetic aberrations are associated with disease progression in chronic myeloid leukemia (CML). This study was conducted to determine the type and frequency of these aberrations and their relationship...
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Two Concurrent Chromosomal Aberrations Involving Three-way t(3;21;8)(p21;q22;q22) and Two-way t(2;11)(q31;p15) Translocations in a Case of de novo Acute Myeloid Leukemia

Park GC, Cho EH, Kang SH, Jang SJ, Moon DS, Park G

One of the most frequent structural chromosomal anomaly is t(8;21)(q22;q22) that occurs in approximately 5-15% of all acute myeloid leukemia (AML). However, t(3;21)(p21;q22) and t(2;11)(q31;p15) translocations are rarely reported in...
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Screening for chromosomal abnormalities using combined test in the first trimester of pregnancy

Park SY, Jang IA, Lee MA, Kim YJ, Chun SH, Park MH

OBJECTIVE: This study was designed to review the screening performance of combined test at the Ewha Womans University Mokdong hospital. METHODS: All women admitted for routine antenatal care between January 1st...
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Inadvertent Transmission of a Donor's Constitutional Chromosome Abnormality after Hematopoietic Stem Cell Transplantation

Yun J, Jo HH, Jeon BR, Lee YK, Kim CK, Park SK, Hong DS

A pre-transplant screening work-up of donors for allogeneic hematopoietic stem cell transplantation (HSCT) is essential. Inadvertent transmission of malignancy from donors with subclinical diseases to recipients has been reported recently...
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Systemic Epstein-Barr Virus-Positive T-cell Lymphoproliferative Disease of Childhood Presenting as Hemophagocytic Lymphohistiocytosis with Chromosomal Abnormalities

Yang N, Chung WS, Mun YC, Huh J

Epstein-Barr virus (EBV)-positive T-cell lymphoproliferative disease (EBV+ T-cell LPD) is characterized by a clonal proliferation of T-cells, which may trigger hemophagocytic lymphohistiocytosis (HLH). Chromosomal abnormalities in patients with HLH are...
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Second-trimester fetal genetic ultrasonography to detect chromosomal abnormalities

Hong SY

Genetic ultrasonography refers to the evaluation of risk of chromosomal abnormalities via various soft sonographic markers. Although the maternal serum test is the primary screening method for chromosomal abnormalities, genetic...
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Characteristics of hematologic malignancies with coexisting t(9;22) and inv(16) chromosomal abnormalities

Han E, Lee H, Kim M, Kim Y, Han K, Lee SE, Kim HJ, Kim DW

BACKGROUND: The coexistence of t(9;22)(q34;q11.2) and inv(16)(p13q22) chromosomal abnormalities is extremely uncommon, and only a small number of such cases have been reported. Here, we characterized 7 cases of hematologic...
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The Association between Cytogenetic Abnormalities and Clinical Outcomes Based on Prognostic Factors of the Children Cancer Group (CCG) in Pediatric Patients with Acute Leukemia: Two Institutional Retrospective Studies

Bae JJ, Jang YS, Kim JY, Lim YJ, Park HK, Han JY, Lee YH

BACKGROUND: We investigated the incidence of cytogenetic abnormalities as well as the correlation of the cytogenetic abnormalities and clinical outcomes based on the prognostic factors of the Children Cancer Group...
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Cytogenetic abnormalities in patients with reproductive dysfunction

Yun JS, Jang SK, Choi OH

  • KMID: 2273132
  • Korean J Obstet Gynecol.
  • 2007 May;50(5):760-768.
OBJECTIVE: The aim of this study was to investigate the relationship between chromosome abnormalities and male or female reproductive dysfunction and to be convinced of the role of pericentric inversion...
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A Case of Myelodysplastic Syndrome Associated with an Isolated del(5q) Chromosomal Abnormality Showing Poor Prognosis

Chung HJ, Park CJ, Chi HS, Jang S, Seo EJ, Lee JH

Typical myelodysplastic syndrome (MDS) associated with isolated del(5q) consists of an interstitial deletion of the band between q13 and q33 on chromosome 5. Generally, patients with isolated deletion 5q have...
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Analysis of Chromosomal Aberrations in Head and Neck Squamous Cell Carcinoma Cell Lines using CGH

Park SY

  • KMID: 1510225
  • Korean J Anat.
  • 2006 Dec;39(6):515-522.
The knowledge about chromosomal aberrations manifestated in cancer has been spotlighted recently, and these studies are important for the development of cancer diagnosis and evaluation of prognosis. Purpose of this...
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Incidence and Types of Constitutional Chromosomal Abnormalities in Patients with Hematologic Malignancies

Huh J, Chung W

BACKGROUND: It is important to distinguish between the constitutional and acquired chromosomal abnormality in bone marrow of the patients with the hematologic malignancies, since the constitutional chromosomal abnormality will be...
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Analysis of Chromosomal Aberrations in Thyroid Papillary Carcinomas Using Comparative Genomic Hybridization (CGH)

Kim JY, Kim HS, Park SY, Shin YR, Go YM, Kim HK, Lee DW, Chung SM

  • KMID: 2276517
  • Korean J Otolaryngol-Head Neck Surg.
  • 2005 Nov;48(11):1369-1376.
BACKGROUND AND OBJECTIVES: Cancer of the thyroid is the sixth common cancer in Korea, and fourth common among the Korean women, in particular. Aming the prevalent carcinomas of thyroid, the...
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Clinical significance of chromosomal abnormality in multiple myeloma

Kim KT, Paik JH, Lee CJ, Kim JH, Bae YZ, Seo BG, Kwon HC, Oh SY, Kim SH, Kim JS, Han JY, Kim HJ

  • KMID: 1984663
  • Korean J Med.
  • 2005 Sep;69(3):304-312.
BACKGROUND: Multiple myeloma is a clonal B-cell malignancy manifested by the accumulation of terminally differentiated plasma cells. The disease is characterized by clinical heterogeneity, with survival ranging from a few...
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The availability of ultrasonography as the method for early detection of fetal chromosomal abnormalities

Ha JA, Kim YH, Kim CH, Cho MK, Kim KM, Kim JW, Song TB

  • KMID: 2272648
  • Korean J Obstet Gynecol.
  • 2005 Aug;48(8):1876-1882.
OBJECTIVE: For the early detection of fetal chromosomal abnormalities in highpregnancy, most obstetricians have performed the prenatal fetal ultrasonogram as an obstetrical diagnostic tool. METHODS: Fetal ultrasonogram and fetal chromosomal analysis...
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Analysis of Chromosomal Aberrations in Lung Cancer Cell Line, NCI-H1373

Park SY

  • KMID: 1564266
  • Korean J Anat.
  • 2005 Apr;38(2):145-151.
The cytogenetic analysis of recurring chromosomal aberrations play an important part to decide pathogenesis and prognosis of cancers. However, due to difficulties culturing tumor cells and complexity associated with the...
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