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A Karyotype Study in Chiroptera (Bats)

Oh YK

The bat (Chiroptera) is the only mammal that is able to fly as birds do and forms a peculiar taxonomic group in that the diploid number of chromosomes seldom are...
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Chromosomes of the liver fluke, Clonorchis sinensis

Park GM, Im K, Huh S, Yong TS

A karyological study was carried out in order to compared the chromosome numbers, chromosome morphologies and karyotypes of the oriental liver fluke, Clonorchis sinensis (Trematoda: Opisthorchiidae), collected from Korea and...
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Marker Chromosomes in Korean Patients: Incidence, Identification and Diagnostic Approach

Woo HY, Cho HJ, Kong SY, Kim HJ, Jeon HB, Kim EC, Park H, Kim YJ, Kim SH

The identification of marker chromosomes is important for genetic counseling. However, the origin or composition can rarely be defined with conventional cytogenetic technique alone. In this study, we investigated the...
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Cytogenetic Analysis of Squamous Cell Carcinoma of the Lung

Jo SJ

  • KMID: 2030733
  • Korean J Anat.
  • 1997 Oct;30(5):567-574.
The cytogenetic study of 3 cases of squamous cell carcinoma of the lung was performed to identify chromosomal abnormalities. All tumor cells were hypodiploid state on the average. Specicfic chromosomal...
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A case of prenatally diagnosed Non-15, Non-22 marker chromosome

Song SR, Song JH, Song JH, Jung YW, Lee SS, Kim MH

  • KMID: 2272554
  • Korean J Obstet Gynecol.
  • 2005 Feb;48(2):480-483.
Midtrimester genetic amniocentesis is an important diagnostic tool in prenatal genetic diagnosis and counseling. We can identify karyotypes with metaphase chromosome analysis of cultured amniocytes. Marker chromosomes are defined as...
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A cytogenetic study on human intestinal trematodes of the genus Metagonimus (Digenea: Heterophyidae) in Korea

Lee SU, Huh S, Park GM, Chai JY

In order to analyze chromosome numbers and karyotypes of intestinal trematodes belonging to the genus, Metagonimus, the gonad tissues of M. takahashii, M. miyatai, and M. yokogawai were prepared...
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Phylogenetically interrelated ETS genes, ETV1, ERM and E1A-F locate on different chromosomes

Jeon IS, Shapiro DN

ETV1, ERM and E1A-F are members of the multigene ETS domain containing a class of transcription factors, first identified in the genome of the avian retrovirus E26. Based upon...
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A Case of Ring Chromosome 14 Syndrome Presenting with Intractable Epilepsy

Kim MJ, Yu HJ, Lee J, Lee M

  • KMID: 2008771
  • J Korean Epilepsy Soc.
  • 2012 Jun;16(1):33-36.
Ring chromosome 14 syndrome is a rare cytogenetic disorder characterized by typical facial appearance, developmental delay, and intractable epilepsy. There have been about 50 reported cases in the world and...
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A Case with Balanced Chromosome Rearrangement Involving Chromosomes 9, 14, and 13 in a Woman with Recurrent Abortion

Kim SK, Kim HJ, Yang YH, Kim IK, Bai SW, Kim JY, Park KH, Cho DJ, Song CH

A phenotypically normal couple was referred for cytogenetic evaluation due to three consecutive first-trimester spontaneous abortions. Chromosomal analysis from peripheral blood was performed according to standard cytogenetic methods using G-banding...
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A Case of Azoospermia Associated with Y - Autosome Translocation

Lee SH, Yoon TK, Cha KY, Kwak IP, Kim HJ, Nam YS

  • KMID: 2261375
  • Korean J Obstet Gynecol.
  • 1999 Mar;42(3):625-627.
Aneuploidy results from nondisjunction in either the meiotic division of the parents or the early cleavage divisions of the affected individuals. The sex chromosomes show a wide range of viable...
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Analysis of Chromosomal Aberration Induced by Low Dose of Radiation

Yi CJ, Ha SW

  • KMID: 2097431
  • J Korean Soc Ther Radiol.
  • 1993 Dec;11(2):233-240.
Chromosomal aberration analysis, as a basis for biological radiation dosimetry, was performed for radiation dose ranges below 150 cGy. The yield, ratio of lymphocytes with dicentric and/or ring chromosomes, was...
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A Case of 21-Monosomy with Holoprosencephaly(Semilobar Type)

Lee SY, Cho SM

  • KMID: 1606978
  • J Korean Pediatr Soc.
  • 2003 Aug;46(8):831-835.
Holoprosencephaly of unknown definite causes, has been associated with several chromosome abnormalities involving the autosomes and the sex chromosomes. The most commonly reported associations include dup(3p), del(7q), deletions of chromosome...
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Identification of marker chromosomes by reverse painting fluorescence in situ hybridization and comparative genomic hybridization

Kang JK, Cho YH, Kyhm JH, Shin ES, Hoh JK, Chung SR

  • KMID: 2272680
  • Korean J Obstet Gynecol.
  • 2005 Sep;48(9):2125-2139.
OBJECTIVE: Although marker chromosome is defined as an abnormal chromosome in which no part can be identified, derivative chromosomes with structural abnormalities of unknown origin are also called as marker...
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A Rare der(Y)t(Y;1)(q12;q12) in a Patient with Essential Thrombocythemia

Lim HH, Choi JL, Kim BR, Woo KS, Kim KH, Kim JM, Kim SH, Han JY

Among hematologic diseases, structural abnormalities of autosomal chromosomes are well-known, but cases involving the sex chromosomes are uncommon. Duplications of the long arm of chromosome 1 have been reported in...
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Ring Chromosome 5 in Acute Myeloid Leukemia Defined by Whole-genome Single Nucleotide Polymorphism Array

Huh J, Mun YC, Chung WS, Seong CM

Chromosomes forming a corresponding ring cannot be clearly defined by conventional cytogenetics or FISH. Karyotypic analyses using whole-genome single nucleotide polymorphism arrays (SNP-A) may result in the identification of previously...
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Karyotype analysis of Neodiplostomum seoulense

Park GM, Lee SU, Park HY, Huh S

A karyotype analysis of the chromosome of Neodiplostomum seoulense, one of causative agents of human intestinal trematodiasis, was done from the gonad tissue by the squashing method. The chromosome...
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Rarely Observed Jumping Translocation in Spontaneous Abortion

Lee YW, Lee BY, Park JY, Choi EY, Oh AR, Lee SY, Ryu HM, Kang IS, Yang KM, Park SY

  • KMID: 2135616
  • J Genet Med.
  • 2010 Jun;7(1):82-86.
Jumping translocations (JT) are chromosomal rearrangements involving one donor chromosome and several recipient chromosomes. While JTs are frequently observed as acquired chromosomal abnormalities in hematologic malignancies, constitutional JTs are only...
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Genentics in Rheumatoid Arthritis

Lee HS

  • KMID: 2168057
  • Hanyang Med Rev.
  • 2005 May;25(2):13-20.
The understanding of genetic factors contributed to the susceptibility or severity of rheumatoid arthritis (RA) might give new insights into the pathways involved in disease pathogenesis and lead to the...
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Periodic Explosive Expansion of Human Retroelements Associated with the Evolution of the Hominoid Primate

Kim TM, Hong SJ, Rhyu MG

Five retroelement families, L1 and L2 (long interspersed nuclear element, LINE), Alu and MIR (short interspersed nuclear element, SINE), and LTR (long terminal repeat), comprise almost half of the human...
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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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