Skip Navigation
Skip to contents
Filter

ARTICLE TYPE

PUBLICATION DATE

8 results
Display

Six-years' Experience of Pseudomosaicism and Maternal Cell Contamination in Cultured Amniocytes

Moon SY, Jee BC, Kim SH, Oh SK, Park JS, Choi YM

  • KMID: 1536940
  • J Genet Med.
  • 1999 Dec;3(1):25-28.
PURPOSE : To present our experiences in pseudomosaicism or maternal celi contamination in genetic mid-trimester amniocentesis confirmed through percuraneous umbilical blood sampling. METHODS : From 1992 to 1997, repeated cytogenetic evaluation...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Genetic Variation in Exon 3 of Human Apo B mRNA Editing Protein (apobec-1) Gene

Hong SH, Song JH, Kim JQ

  • KMID: 1536938
  • J Genet Med.
  • 1999 Dec;3(1):15-20.
We have investigated the genetic variation in the human apo B mRNA editing protein (apobec-1) gene. Exon 3 of the apobec-1 gene was amplified by polymerase chain reaction. After detection...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Development of Tetracycline-regulated Adenovirus Expression Vector System

Son KH, Lee SH, Kim JS, Choi JJ, Lee JH

  • KMID: 1536942
  • J Genet Med.
  • 1999 Dec;3(1):33-36.
Recombinant adenovirus vector systems with strong promoters have been used to achieve high level production of recombinant protein. However, this overexpression system cause some problems such as disturbance of cell...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
The Study of Synergy between the BchE-k Variant and the ApoE Gene in the Alzheimer Dementia of the Korean Population

Shin ES, Yoon SR, Choi SK, Kim SY

  • KMID: 1536941
  • J Genet Med.
  • 1999 Dec;3(1):29-32.
The Apolopoprotein E type 4 allele (ApoE epsilon 4) is genetically associated with the common late anset familial and sporadic forms of Alzheimer's disease. The BchE-k variant, which is the...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Familial Chromosome No. 9 Pericentic Inversion Producing Scimitar Syndrome

Kim JW, Kim YY, Shin JC, Lee WB

  • KMID: 1536935
  • J Genet Med.
  • 1999 Dec;3(1):1-4.
Scimitar syndrome is a rare congenital anomaly that is characterized by hypoplasia of the right lung and the right pulmonary artery with anomalous pulmonary venous drainage to the inferior vena...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Frepuency of the Angiotensin - Converting Enzyme (ACE) Gene Polymorphism in the General Population and the Elite Endurance Students in Korea

Choung HJ, Yoon SR, Choi SK

  • KMID: 1536937
  • J Genet Med.
  • 1999 Dec;3(1):11-14.
Recintly it was reported that Insertion / Deletion polymorphism in the gene coding for Angiotensin Converting Enzyme (ACE) is asscoiated with human capacity for physical performance. This study was performed...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Molecular Study of X-Chromosome Mosaicism in Turner Syndrome Patients using DNAs Extracted from Archives Cytogenetic Slides

Cho EH, Kim JW, Kim YM, Ryu HM, Park SY

  • KMID: 1536939
  • J Genet Med.
  • 1999 Dec;3(1):21-24.
To study the X chromesome masaicism in the cytogenetically pure 45,X Turner syndrome patients, we applied PCR technique using DNAs extracted from archived cytogenetic slides. We amplified the DNAs using...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Molecular Analysis of the Y Chromosome in a 46,XY Female Phenotype

Kim JW, Kim TJ, Park SY, Nam SA, Jun JY

  • KMID: 1536936
  • J Genet Med.
  • 1999 Dec;3(1):5-10.
This is a case report of 46,XY female phenotype (46,XY karyotype, no pubic hair, blind vagina and absence of uterus)in an 18-year-old patient. To confirm whether a Y chromosome has...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr