- Current Status and Future Clinical Applications of Array.based Comparative Genomic Hybridization
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Yim SH, Chung YJ
- KMID: 2053076
- Genomics Inform.
- 2004 Sep;2(3):113-120.
No abstract available. -
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- Array-based Comparative Genomic Hybridization and Its Application to Cancer Genomes and Human Genetics
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Cho EK
- KMID: 2005738
- J Lung Cancer.
- 2011 Dec;10(2):77-86.
- doi: 10.6058/jlc.2011.10.2.77
Microarray comparative genomic hybridization (CGH) has proven to be a specific, sensitive, and rapid technique, with considerable advantages compared to other methods used for analysis of DNA copy number changes.... -
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- A Case of Identification of Marker Chromosome by comparative genomic hybridization and fluorescence in situ hybridization
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Shin SY, Jeon YM, Ihm CH, Kim MH, Koo SH, Park JW, Kwon KC, Park YM
- KMID: 2226047
- Korean J Clin Pathol.
- 2001 Aug;21(4):310-313.
Comparative genomic hybridization (CGH) has been used to identify deletions and amplifications, particularly in neoplastic samples. CGH provides a new possibility searching genomes for imbalances of genetic material. We described... -
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- Next generation sequencing and array-based comparative genomic hybridization for molecular diagnosis of pediatric endocrine disorders
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Fukami M, Miyado M
- KMID: 2383902
- Ann Pediatr Endocrinol Metab.
- 2017 Jun;22(2):90-94.
- doi: 10.6065/apem.2017.22.2.90
Next-generation sequencing (NGS) and array-based comparative genomic hybridization (array CGH) have enabled us to perform high-throughput mutation screening and genome-wide copy number analysis, respectively. These methods can be used for... -
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- Chromosomal gains and losses in primary ovarian carcinomas by comparative genomic hybridization
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Cho SH, Kim MH, Lee NW, Kim YT, Lee KW
- KMID: 2020113
- Korean J Obstet Gynecol.
- 2003 Jan;46(1):38-43.
OBJECTIVE: Comparative genomic hybridization was performed to evaluate DNA sequence copy number changes in human ovarian carcinomas from paraffin-embedded tissue blocks. PATIENTS AND METHODS: DNA from 20 cases of primary ovarian... -
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- Diagnostic approach for genetic causes of intellectual disability
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Yim SY
- KMID: 2055583
- J Genet Med.
- 2015 Jun;12(1):6-11.
- doi: 10.5734/JGM.2015.12.1.6
Intellectual disability (ID) is the most common disability among people under the age of 20 years. In the absence of obvious non-genetic causes of ID, the majority of cases of... -
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- A de novo Proximal 6q Deletion Confirmed by Array Comparative Genomic Hybridization
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Woo KS, Kim JE, Kim KE, Kim MJ, Yoo JH, Ahn HS, Shaffer LG, Han JY
- KMID: 1096824
- Korean J Lab Med.
- 2010 Feb;30(1):84-88.
- doi: 10.3343/kjlm.2010.30.1.84
Deletions of chromosome 6q, particularly in the proximal region, are relatively rare. Here, we report on a de novo interstitial deletion of (6)(q13q16.2) in a girl with facial dysmorphism, congenital... -
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- 14q32.33 Deletion Identified by array-CGH in a 5-year old-girl with Seizure
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Cheon CK, Park SJ, Choi OH
- KMID: 1851093
- J Genet Med.
- 2011 Jun;8(1):62-66.
- doi: 10.5734/JGM.2011.8.1.62
Deletions of 14q including band 14q32.33 are uncommon. Patients with terminal deletions of chromosome 14 usually share a number of clinical features. By molecular techniques (array comparative genomic hybridization (CGH)... -
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- Genetic Alterations in Colorectal Carcinoma Detected by Comparative Genomic Hybridization
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Park SJ, Park MI, Koo SH, Koo JY
- KMID: 2038323
- Korean J Gastroenterol.
- 2002 Apr;39(4):275-283.
BACKGROUND/AIMS: Comparative genomic hybridization (CGH) is a new powerful technique for the molecular cytogenetic analysis of cancer. METHODS: Twenty-five colorectal carcinomas were screened for chromosomal aberrations using CGH. RESULTS: All carcinomas had... -
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- Advantages of Array Comparative Genomic Hybridization Using Buccal Swab DNA for Detecting Pallister-Killian Syndrome
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Bertini V, Gana S, Orsini A, Bonuccelli A, Peroni D, Angelo V
- KMID: 2425984
- Ann Lab Med.
- 2019 Mar;39(2):232-234.
- doi: 10.3343/alm.2019.39.2.232
No abstract available. -
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- A study on the chromosomal aberrations in Korean intrahepatic cholangiocarcinomas with comparative genomic hybridization
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Choi SH, Sohn TS, Joh JW, Kim SJ, Heo JS, Kim YI, Lee KS, Cho YH
- KMID: 2244416
- Korean J Hepatobiliary Pancreat Surg.
- 1999 Aug;3(2):77-88.
AIMS AND METHOD: Comparative genomic hybridization serves as a screening test for regions of copy number changes in tumor genomes. I have applied the technique to map DNA losses and... -
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- Duplication of intrachromosomal insertion segments 4q32-->q35 confirmed by comparative genomic hybridization and fluorescent in situ hybridization
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Kim JW, Park JY, Oh AR, Choi EY, Ryu HM, Kang IS, Koong MK, Park SY
- KMID: 1743682
- Clin Exp Reprod Med.
- 2011 Dec;38(4):238-241.
- doi: 10.5653/cerm.2011.38.4.238
A 35-year-old man with infertility was referred for chromosomal analysis. In routine cytogenetic analysis, the patient was seen to have additional material of unknown origin on the terminal region of... -
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- Genomic Imbalances in Ependymoma by Degenerate Oligonucleotide Primed PCR-Comparative Genomic Hybridization
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Park SH, Kim GJ, Kim MK, Kim H, Suh YL, Park SH
- KMID: 2275493
- Korean J Pathol.
- 2004 Jun;38(3):133-137.
BACKGROUND: The most consistent chromosomal abnormality in ependymomas, is loss of 22q (17-75%) and gain of 1q (0-50%). However, significance of this abnormality is uncertain. METHODS: Genomic imbalances in 27 Korean... -
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- Overgrowth Syndrome with 9q22.3 Microdeletion Detected by Microarray Comparative Genomic Hybridization
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Park YJ, Park SB, Kim SM, Chae YJ, Kim JD, Jung CL
- KMID: 1802887
- Neonatal Med.
- 2014 Nov;21(4):264-269.
- doi: 10.5385/nm.2014.21.4.264
Microdeletion of 9q22.3 is a rare chromosomal disorder characterized by body overgrowth, facial dysmorphic features and psychomotor delay. The presence of genomic microdeletion or microdu-plication can not be identified by... -
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- Degenerate oligonucleotide primed PCR for the application to comparative genomic hybridization
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Kim SH, Kang SJ, Kim MS, Lee EJ, Lee JH, Choi C, Kim BY
- KMID: 2092713
- Korean J Anat.
- 2000 Feb;33(1):41-48.
Degenerate oligonucleotide primed PCR is an useful technique to amplify whole genome and its the applications for fluorescent in situ hybridization and comparative genomic hybridization (CGH) were reported. For the... -
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- Analysis of Chromosomal Aberrations in Lung Cancer Cell Line, NCI-H1373
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Park SY
- KMID: 1564266
- Korean J Anat.
- 2005 Apr;38(2):145-151.
The cytogenetic analysis of recurring chromosomal aberrations play an important part to decide pathogenesis and prognosis of cancers. However, due to difficulties culturing tumor cells and complexity associated with the... -
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- A New Prenatal Diagnosis of Fetal Cells Isolation from Maternal Peripheral Blood -Using Comparative Genomic Hybridization by Microdissection
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Yang YH, Kim SH, Kim SK, Park YW, Cho JS, Kim IK, Choi JR, Kim MS
- KMID: 2262620
- Korean J Obstet Gynecol.
- 2002 Feb;45(2):213-219.
OBJECTIVE: The objective of this study was to determine the clinical use of CGH (comparative genomic hybridization) for detection of fetal aneuploidy from fetal cells (nucleated red blood cells, nRBCs)... -
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- DNA Gains and Losses of Chromosome in Laryngeal Squamous Cell Carcinoma Using Comparative Genomic Hybridization
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Keser I, Toraman AD, Ozbilim G, Guney K, Luleci G
- KMID: 1782943
- Yonsei Med J.
- 2008 Dec;49(6):949-954.
- doi: 10.3349/ymj.2008.49.6.949
PURPOSE: A larynx squamous cell carcinoma (LSCC) is one of the most common forms of cancer and may exhibit various complex karyotypes. MATERIALS AND METHODS: We used comparative genomic hybridization... -
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- RAN-aCGH: R GUI Tools for Analysis and Visualization of an Array-CGH Experiment
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Kim S, Kim BS
- KMID: 2166270
- Genomics Inform.
- 2007 Sep;5(3):137-139.
RAN-aCGH is an R GUI tool for the analysis and visualization of array comparative genomic hybridization (array-CGH) experiments. The tool consists of data-loading, preprocessing for missing data, several methods for... -
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- Preimplantation genetic diagnosis
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Kim JY, Lee HS, Kang IS
- KMID: 2195126
- J Korean Med Assoc.
- 2015 Nov;58(11):979-988.
- doi: 10.5124/jkma.2015.58.11.979
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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