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Clinical Application of Preimplantation Genetic Diagnosis (PGD)

Kim JY, Kang IS

  • KMID: 1483346
  • Korean J Reprod Med.
  • 2008 Mar;35(1):19-38.
No abstract available.
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Preimplantation Genetic Diagnosis

Lee SH, Cho SW, Han JH, Cha KE, Kay CW, Kwak IP, Lee EJ, Yoon TK, Cha KY

  • KMID: 2261200
  • Korean J Obstet Gynecol.
  • 1998 Dec;41(12):2913-2916.
No abstract available.
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Recent Trends in Preimplantation Genetic Diagnosis (PGD)

Kim JY, Kang IS

  • KMID: 2272722
  • Korean J Obstet Gynecol.
  • 2005 Nov;48(11):2493-2509.
Preimplantation genetic diagnosis (PGD) provides practical option to prevent the termination of pregnancy and miscarriage in couples with high risk of genetic disease or recurrent spontaneous abortion. In balanced chromosomal...
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Reliability of the Single Cell PCR analysis for Preimplantation Genetic Diagnosis of Single Gene Disorders

Choi HW, Lee HS, Lim CK, Koong MK, Kang IS, Jun JH

  • KMID: 1772289
  • Korean J Fertil Steril.
  • 2005 Dec;32(4):293-300.
No abstract available.
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Development of Multicolor Fluorescence In Situ Hybridization for Preimplantation Genetic Diagnosis in Human Embryos

Kim SH, Choi SM, Kim HS, Ryu BY, Bang MG, Oh SG, Jee BC, Seo CS, Choi YM, Bae GB, Kim JG, Moon SY, Lee JY

  • KMID: 2036194
  • Korean J Obstet Gynecol.
  • 2000 Dec;43(12):2170-2177.
No abstract available.
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The first successful live birth following preimplantation genetic diagnosis using PCR for type 1 citrullinemia

Cho JH, Kim CH, Lee KH, Jeon IK, Kim JM, Kang BM

Type 1 citrullinemia (CTLN1) is an autosomal recessive inherited metabolic disorder caused by anargininosuccinicnate synthetase deficiency. The patient was a 38-year-old Korean woman who is a carrier for CTLN1 and...
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A Case of Recurrent Spontaneous Abortion Successfully Delivered by Using Preimplantation Genetic Diagnosis

Nam YS, Lee SH, Oum KB, Lee EJ, Chung HM, Cha KY

  • KMID: 2085148
  • Korean J Fertil Steril.
  • 2000 Sep;27(3):307-311.
OBJECTIVE: To report the successful delivery in a patient of recurrent spontaneous abortion caused by chromosomal abnormality. MATERIAL AND METHOD: Case report. RESULTS: Twelve oocytes were obtained by in vitro fertilization. Of...
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A Case of Successful Pregnancy in Patient with Recurrent Spontaneous Abortion by Preimplantation Genetic Diagnosis Following IVF-ET

Jeong JS, Yeon GS, Chae HD, Cheon YP, Kim CH, Kang BM, Chang YS, Mok JE

  • KMID: 2304573
  • Korean J Fertil Steril.
  • 1998 Aug;25(2):135-140.
It was reported that the etiologies of recurrent spontaneous abortion are immunologic factors, endocrinologic problems, anatomical abnormalities, genetic abnormalities, infection, and unexplained factors. Among those etiologic factors, genetic abnormalities occur...
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Preimplantation Genetic Diagnosis of Chromosomal Abnormality with Clinical Application of Multicolor FISH in Embryos Developed after ICSI in Male Factor Infertile Patients

Kim SH, Choi SM, Kim HS, Ryu BY, Pang MG, Oh SK, Ku SY, Jee BC, Suh CS, Choi YM, Kim JG, Moon SY, Lee JY

  • KMID: 2262088
  • Korean J Obstet Gynecol.
  • 2000 Sep;43(9):1624-1634.
No abstract available.
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Preimplantation Genetic Diagnosis for Single Gene Disorders

Lee HS, Kim MJ, Kang IS

  • KMID: 1473817
  • J Genet Med.
  • 2009 Dec;6(2):131-145.
Preimplantation genetic diagnosis (PGD) has become an assisted reproductive technique for couples who are at risk that enables them to have unaffected baby without facing the risk of pregnancy termination...
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Clinical application of preimplantation genetic diagnosis (PGD) using fluorescence in-situ hybridization to balanced reciprocal or Robertsonian translocation carriers in human IVF-ET program

Jun JH, Song GJ, Kim JW, Park SY, Kim KH, Choi BC, Koong MK, Kang IS, Lim CK, Han MH

  • KMID: 2262031
  • Korean J Obstet Gynecol.
  • 2000 Jul;43(7):1147-1153.
OBJECTIVE: This study was performed to evaluate the efficiency of preimplantation genetic diagnosis (PGD) using fluorescence in-situ hybridization (FISH) in Robertsonian or balanced reciprocal translocation carriers in human IVF-ET programm. METHOD: FISH...
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Birth of a healthy baby after preimplantation genetic diagnosis in a carrier of mucopolysaccharidosis type II: The first case in Korea

Ko DS, Lee SH, Park CW, Lim CK

Mucopolysaccharidosis type II (MPS II) is a rare X-linked recessive lysosomal storage disease caused by mutation of the iduronate-2-sulfatase gene. The mutation results in iduronate-2-sulfatase deficiency, which causes the progressive...
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The Ethical and Legal Considerations on Preimplantation Genetic Diagnosis and Prenatal Diagnosis

Kim JH

  • KMID: 2272988
  • Korean J Obstet Gynecol.
  • 2006 Dec;49(12):2497-2505.
OBJECTIVE: After 'Bioethics & biosafety act' has been enacted since 2005, Preimplantation genetic diagnosis (PGD) for embryo and Prenatal diagnosis (PD) for fetus are regulated by this law. This article...
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Preimplantation genetic diagnosis

Kim JY, Lee HS, Kang IS

Preimplantation genetic diagnosis (PGD) is a technique to examine genetic disease or chromosome abnormalities in single cell biopsied from embryos before implantation to uterus. It allows achieving normal pregnancy by...
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Application of Hot Start PCR Method in PCR-based Preimplantation Genetic Diagnosis

Kim SA, Kang MJ, Kim HS, Oh SK, Ku SY, Choi YM, Jun JK, Moon SY

PURPOSE: To determine a method to improve the efficacy and accuracy of preimplantation genetic diagnosis (PGD) - polymerase chain reaction (PCR), we compared hot start PCR and conventional multiplex nested...
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Prenatal Diagnosis of Duchenne Muscular Dystrophy (DMD) by Multiplex Polymerase Chain Reaction (PCR) with Chorionic Villi

Lee KW, Yoon SW, Chang WS, Kim JY, Lee SH, Lee SJ, Kim SD, Han JS

  • KMID: 2269871
  • Korean J Obstet Gynecol.
  • 1999 Sep;42(9):2028-2032.
OBJECTIVE: To evaluate the efficacy of prenatal multiplex PCR with chorionic villi, in the case of family history of DMD due to exon deletion. METHODS: DNA was extracted when cells'...
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Analysis of haplotype and coamplification PCR of dystrophin gene and Y-specific gene using PEP-PCR in single fetal cells

Choi SK

  • KMID: 1538083
  • J Genet Med.
  • 1998 Mar;2(1):35-40.
Duchenne and Becker muscular dystrophy are the major neuromuscular disorders with X-linked recessive inheritance. Preimplantation sex determination has been generally used to avoid pregnancies with these diseases. However, in order...
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An update of preimplantation genetic diagnosis in gene diseases, chromosomal translocation, and aneuploidy screening

Chang LJ, Chen SU, Tsai YY, Hung CC, Fang MY, Su YN, Yang YS

Preimplantation genetic diagnosis (PGD) is gradually widely used in prevention of gene diseases and chromosomal abnormalities. Much improvement has been achieved in biopsy technique and molecular diagnosis. Blastocyst biopsy can...
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Does blastomere biopsy in preimplantation genetic diagnosis affect early serum beta-hCG levels?

Cho YJ, Kim JY, Song IO, Lee HS, Lim CK, Koong MK, Kang IS

OBJECTIVE: To determine whether the serum beta-human chorionic gonadotropin (hCG) profile following preimplantation genetic diagnosis (PGD) is lower than that of intracytoplasmic sperm injection (ICSI) cycles. METHODS: A total of 129...
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Preimplantation genetic diagnosis for Charcot-Marie-Tooth disease

Lee HS, Kim MJ, Ko DS, Jeon EJ, Kim JY, Kang IS

OBJECTIVE: Preimplantation genetic diagnosis (PGD) is an assisted reproductive technique for couples carrying genetic risks. Charcot-Marie-Tooth (CMT) disease is the most common hereditary neuropathy, with a prevalence rate of 1/2,500....
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