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Partial Trisomy 2q(2q37.3->qter)and Monosomy 7q(7q34->qter) Due to Paternal Reciprocal Translocation 2;7: A Case Report

Lee YH, Ahn JM, Koo DH, Kwon KW, Lee YK, Lee HH, Nam KH, Lee KH

We report an unbalanced translocation involving chromosome 2 and 7 due to a balanced reciprocal translocation 2;7 in the father. The female fetus had a partial trisomy of the long...
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Congenital Monoblastic Leukemia with 9;11 Translocation in Monozygotic Twins: A Case Report

Park SY, Jang JJ, Kim CW, Cho HI, Chi JG

We report an autopsy case of congenital monoblastic leukemia that developed in monozygotic twins. The twin presented with progressive hepatosplenomegaly at 4 weeks after birth. One twin died of massive...
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Chromosome abnormalities in a referred population for suspected chromosomal aberrations: a report of 4117 cases

Kim SS, Jung SC, Kim HJ, Moon HR, Lee JS

A cytogenetic study was performed on 4,117 Korean patients referred for suspected chromosomal abnormalities. Chromosome aberrations were identified in 17.5% of the referred cases. The most common autosomal abnormality was...
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Frequencies of Fetal Chromosomal Abnormalities at Prenatal Diagnosis: 10 years experiences in a single institution

Park SY, Kim JW, Kim YM, Kim JM, Lee MH, Lee BY, Han JY, Kim MY, Yang JH, Ryu HM

We present frequencies of fetal chromosomal abnormalities in 4,907 prenatal cytogenetic examinations at Samsung Cheil Hospital from 1988 to 1997 for 10 yr duration. Prenatal karyotypes were undertaken in 3,913...
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Cloning and expression of rat liver type glucose transporter and translocation by insulin in Chinese hamster ovary cells

Ahn YH, Yoon DJ, Han GS, Lee BG

The 5'- and 3'-side half of liver type glucose transporter (GLUT2) cDNA was amplified from total RNA or mRNA by reverse transcriptase-polymerase chain reaction (RT-PCR). The amplified 5'-side fragment of...
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The effect of genetic counseling on performance of prenatal cytogenetic diagnosis

Kim SK, Kim IK, Kim CK, Yang YH, Park TK, Kim KY

Currently the number of pregnant women who have indications for, but do not receive, prenatal cytogenetic diagnosis is increasing. The purpose of this study was to review the prenatal cytogenetic...
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Detection of t(11;22)(q24;q12) translocation of Ewing's sarcoma in paraffin embedded tissue by nested reverse transcription-polymerase chain reaction

Park YK, Chi SG, Park HR, Yang MH, Unni KK

Ewing's sarcoma is a poorly characterized malignant tumor with a relatively uniform histologic appearance, made up of densely packed small cells with round to oval nuclei, without distinct cell...
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Prenatal detection of de novo inversion of chromosome 9 with duplicated heterochromatic region and postnatal follow-up

Kim JJ, Rhee HS, Chung YT, Park SY, Choi SK

  • KMID: 755041
  • Exp Mol Med.
  • 1999 Sep;31(3):134-136.
We report the first de novo case of a heterochromatic duplication on the long arm of the chromosome 9, which then was pericentrically inverted at p11q13. This condition was detected prenatally and...
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Cytogenetic Studies of the Leukocytes of Couples with Habitual Abortions

Hahn S, Kim DS

Karyotypes were prepared from peripheral blood leukocytes in 18 couples with his-tories of habitual abortions. The Standard chromosome analysis and G-banding techniques were studied. The abnormal karyotypes seen were one...
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Real-time PCR analysis of the apoptosis related genes in ATRA treated APL t(15;17) patients

Savli H, Sirma S, Nagy B, Aktan M, Dincol G, Ozbek U

  • KMID: 1093619
  • Exp Mol Med.
  • 2003 Oct;35(5):454-459.
All-trans retinoic acid (ATRA) treatment of the acute promyelocytic leukemia (APL) have subsequently resulted in cell apoptosis, but the molecular mechanism of this effect remains elusive. In order to understand...
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De novo Chromosomal Aberrations in the Fetus; Genetic Counseling and Clinical Outcome

Park SY, Lee BY, Kim YM, Kim JM, Lee MH, Kim JW, Cho EH, Park JY, Lee YH, Yang JH, Kim MY, Han JY, Ryu HM

The aim of this study was to examine the incidence and clinical outcome of de novo chromosomal aberrations retrospectively and provide useful data for genetic counseling in the prenatal cytogenetic...
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