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Cytogenetic Analysis of 467 Cases of Amniocetesis

Hwong SK, Son SM, Lee JG, Lee MG, Bae YC, Han YT

  • KMID: 2071989
  • Korean J Perinatol.
  • 1999 Jun;10(2):189-193.
OBJECTIVE: The study of 467 cases of amniocentesis have been done at the department of Genetics, Taegu Cheil Hospital from Oct. 1997 to May 1999 for the purpose of analysis...
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Clinical efficiency of the measurement of fetal nuchal translucency and Doppler examination of ductus venosus as a screening tool for chromosomal abnormalities

Na SH, Koo BS

  • KMID: 2273660
  • Korean J Obstet Gynecol.
  • 2009 Jan;52(1):61-67.
OBJECTIVE: To evaluate the efficiency of the measurement of fetal nuchal translucency (FNT) and ductus venosus Doppler examination (DV Doppler) as a screening tool for chromosomal abnormalities. METHODS: FNT measurement and...
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Chromosomal Analysis of Abortus Chorionic Villi in Missed Abortion

Choi YY, Kim HM, Son YS, Kim JI

  • KMID: 2261108
  • Korean J Obstet Gynecol.
  • 1998 Aug;41(8):2097-2101.
Chromosomal analysis was done on abortus chorionic villi samples obtained 20 women with history of missed abortion from Sep, 1995, to Nov, 1997. The results of this study revealed abnormal...
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A Cytogenetic Survey of the Mentally Retarded Children

Ju KS, Lee HK

  • KMID: 2261774
  • Korean J Obstet Gynecol.
  • 2000 Jan;43(1):11-16.
OBJECTIVE: A cytogenetic survey of the mentally retarded children in Seoul City Welfare Center for the Mentally Retarded and St Peter school has been undertaken. METHODS: The chromosome analysis was...
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Cytogenetic and clinical analysis of midtrimester amniocentesis

Choi SJ, Kim WS, Kim JU, Lee ES, Cho EH, Kim SH, Roh CR, Kim JH

  • KMID: 1594558
  • Korean J Obstet Gynecol.
  • 2005 Jun;48(6):1420-1430.
OBJECTIVE: To analyze the clinical features and cytogenetic results of midtrimester amniocentesis. METHODS: We reviewed retrospectively medical records of 1,622 women who received amniocentesis from 1998 to 2003. The maternal age...
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Clinical Analysis of 739 Cases of Midtrimester Amniocentesis

Chun YY, Ku JY, Song JW, Kim BS, Bae YY, Sun JG, Kee KS

  • KMID: 2280555
  • Korean J Perinatol.
  • 2005 Jun;16(2):146-153.
OBJECTIVE: To analyze the change of indications and chromosomal abnormalities according to patient's age and indications in midtrimester genetic amniocentesis. METHODS: This study was reviewed 739 genetic amniocentesis results which...
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Multicenter Trial of Aberrations of Chromosomes in Abortuses, Chorionic villi, Amniocytes, and Fetal Blood Cells

Jun JK, Choe J, Choi YM, Hwang DY, Oh SK, Moon SY, Lee JY

  • KMID: 2262039
  • Korean J Obstet Gynecol.
  • 2000 Jul;43(7):1200-1206.
OBJECTIVES: Chromosomal anomalies are common disease entity among genetic diseases. But there are scanty reports about the status of chromosomal abnormalities in Korean. In addition, the comprehensive multi-center study of...
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Cytogenetic Aberration Analysis of Midtrimester Amniotic Fluid

Kim GJ, Choi SR, Kim SY, Yoon SJ, Han EH, Ahn JR, Choi YD, Lee SP, Whang BC, Lee ED, Choi SH

  • KMID: 2270302
  • Korean J Obstet Gynecol.
  • 2002 Jun;45(6):1040-1044.
OBJECTIVE: To analyze cytogenetic results of prenatal genetic amniocentesis. METHODS: From January 1997 to December 2000, We analyzed 1,390 cases of midtrimester amniocentesis which were done at Gil medical center...
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Prenatal Diagnosis with Genetic Amniocentesis

Shin DY, Kong MS, Park MI, Chung SR, Hwang YY, Cho YH, Choi KH

  • KMID: 2280510
  • Korean J Perinatol.
  • 1999 Sep;10(3):375-382.
OBJECTIVE: Amniocentesis for the diagnosis of prenatal genetic abnormalities is now the standard care for women who are at special risk. because the application of population-based maternal serum screening to...
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Clinical Outcomes of Increased Nuchal Translucency in Three Years

Kim MH, Park SH, Cha SH, Kim YJ, Moon MJ, Chung JH, Choi JS, Kim JO, Shin JS, Ahn HK, Han JY, Ryu HM, Yang JH, Choi KH, Lee YH, Kim MY

  • KMID: 2272185
  • Korean J Obstet Gynecol.
  • 2003 Nov;46(11):2151-2155.
OBJECTIVE: To evaluate the relationship between increased nuchal translucency (NT) and abnormal pregnancy outcomes. METHODS: From January 1999 to December 2001, The 298 fetuses of increased nuchal translucency (>or=2.5 mm) in...
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Prenatal Diagnosis with Genetic Amniocentesis

Shin DY, Kong MS, Park MI, Chung SR, Hwang YY, Cho YH, Choi KH

  • KMID: 2280507
  • Korean J Perinatol.
  • 1999 Sep;10(3):353-359.
OBJECTIVE: Amniocentesis for the diagnosis of prenatal genetic abnormalities is now the standard care for women who are at special risk. because the application of population-based maternal serum screening to...
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Clinical Investigation of Primary Amenorrhea

Rhee JH

  • KMID: 2270310
  • Korean J Obstet Gynecol.
  • 2002 Jun;45(6):1045-1051.
OBJECTIVE: To assess the etiologic diagnosis of primary amenorrhea and review the clinical significance in management of primary amenorrhea. METHODS: To make the accurate etiologic diagnosis of primary amenorrhea, karyotype,...
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Clinical Significance of Amniotie Fluid Cell Culture Failure

Lee SG, Lee IS, Lee KH, Lee HH, Choi KH, Kim DH, Yang HK, Lee SK

  • KMID: 1553259
  • Korean J Perinatol.
  • 1999 Mar;10(1):24-29.
The reports of all amniocentesis samples received in our cytogenetic laboratory from 1986 to 1998 were reviewed to identify cases in which culture failure of amniocytes occurred. Medical records were...
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Amylase-Producing IgG Kappa Type Multiple Myeloma

Kim KC, Lee HS, Jang YS, Lee WS, Son HS

  • KMID: 2083446
  • Korean J Hematol.
  • 2002 May;37(2):158-160.
Amylase-producing multiple myeloma is a rare disorder and has poor prognosis. Its characteristics are elevation of salivary type amylase, extensive extramedullary spread, extensive bone destruction, shorter survival time, and abnormal...
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Clinical and Cytogenetic Analysis of Midtrimester Amniocentesis

Lee JG, Chung KH, Kang BH, Noh HT, Rhee YE, Gu SH

  • KMID: 2272394
  • Korean J Obstet Gynecol.
  • 2004 Oct;47(10):1872-1879.
OBJECTIVE: To analyze the indications, clinical features, cytogenetic results and complications of amniocentesis and to determine the efficacy of antenatal genetic amniocentesis. METHODS: We analyzed retrospectively maternal age, gestational age, indications,...
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Clinical significance of fetal nuchal translucency during early pregnancy

Shim JY, Hwang JY, Kim SK, Koo BS, Won HS, Lee PR, Kim A

  • KMID: 2272565
  • Korean J Obstet Gynecol.
  • 2005 Apr;48(4):875-883.
OBJECTIVE: To examine the significance of fetal nuchal translucency during early pregnancy in detection of chromosomal abnormality and major cardiac defect METHODS: Between Jul 1998 and Jul 2002, ultrasound examination was...
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The clinical phenotype of the derivative (8)t(7;8)(q22;p23.3) in two siblings

Kim YO, Cho YK, Song ES, Han DK, Choi IS, Baek HJ, Kim CJ, Woo YJ, Choi YY

We report on 2 siblings with a partial trisomy of 7q (7q22-->qter) and concomitant partial monosomy of 8p (8p23.3-->pter), which were shown by FISH using probes located at the telomere...
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Clinical Analysis of Prenatal Cytogenetic Diagnoses: Four-year Experience at Asan Medical Center

Shim JY, Kim SH, Kim JS, Ahn SM, Seo EJ, Yoo HW, Kim GH, Lee JY, Choi EY, Won HS, Suh DS, Lee PR, Kim A

  • KMID: 2019485
  • Korean J Obstet Gynecol.
  • 2004 Mar;47(3):487-494.
OBJECTIVE: To review and evaluate a total of 2,372 cases of prenatal cytogenetic diagnoses at Asan Medical Center from 1999 to 2002. METHODS: We reviewed the medical records of the patients...
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A Cytogenetic Analysis of Abortus with Spontaneous Abortion

Hwang SM, Kwon KH, Yoon KA, Oh SK

  • KMID: 2244892
  • J Genet Med.
  • 2009 Jun;6(1):62-66.
PURPOSE: Chromosomal abnormalities of abortuses have been used to investigate common etiologies of spontaneous abortion, but the frequencies and types of spontaneous abortions have demonstrated considerable variation among different countries...
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Clinical analysis of chorionic villus sampling

Kim JS, Won HS, Baek SJ, Choi ES, Shim JY, Kim SH, Kim JH, Lee PR, Kim A

  • KMID: 2280763
  • Korean J Perinatol.
  • 2008 Mar;19(1):24-36.
OBJECTIVE: The aims of this study were 1) to evaluate the indications of chorionic villus sampling CVS) and the positive predictive value for fetal chromosomal abnormalities, 2) to evaluate the...
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