- Prenatal detection of de novo inversion of chromosome 9 with duplicated heterochromatic region and postnatal follow-up
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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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- Chromosome abnormalities in a referred population for suspected chromosomal aberrations: a report of 4117 cases
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Kim SS, Jung SC, Kim HJ, Moon HR, Lee JS
- KMID: 1731309
- J Korean Med Sci.
- 1999 Aug;14(4):373-376.
- doi: 10.3346/jkms.1999.14.4.373
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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- Myelodysplastic syndrome that progressed to acute myelomonocytic leukemia with eosinophilia showing peculiar chromosomal abnormality: a case report
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Kim SH, Suh CW, Choi SJ, Kim JG, Lee JH, Kim SB, Kim SW, Lee KH, Lee JS, Kim WK, Kim SH, Seo EJ, Chi HS
- KMID: 1731321
- J Korean Med Sci.
- 1999 Aug;14(4):448-450.
- doi: 10.3346/jkms.1999.14.4.448
Myelodysplastic syndrome is a closely related group of acquired bone marrow disorders characterized by ineffective and dysplastic hematopoiesis. These clonal disorders frequently progress to acute leukemia. Acute myelomonocytic leukemia with... -
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- Frequencies of Fetal Chromosomal Abnormalities at Prenatal Diagnosis: 10 years experiences in a single institution
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Park SY, Kim JW, Kim YM, Kim JM, Lee MH, Lee BY, Han JY, Kim MY, Yang JH, Ryu HM
- KMID: 1129899
- J Korean Med Sci.
- 2001 Jun;16(3):290-293.
- doi: 10.3346/jkms.2001.16.3.290
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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