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| 1 |
Practical Guidelines for Chromosomal Microarray Analysis for Constitutional Abnormalities: Part I, General and Prenatal
Chang Ahn Seol, Jung-Sook Ha, Dong-Joo Won, In-Suk Kim
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| 2 |
Practical Guidelines for Chromosomal Microarray Analysis for Constitutional Abnormalities: Part II, Reporting and Interpretation
Dongju Won, Chang Ahn Seol, Jung-Sook Ha, In-Suk Kim
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| 3 |
Effects of Copy Number Variations on Developmental Aspects of Children With Delayed Development
Kee-Boem Park, Kyung Eun Nam, Ah-Ra Cho, Woori Jang, Myungshin Kim, Joo Hyun Park
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| 4 |
Using low-coverage whole genome sequencing technique to analyze the chromosomal copy number alterations in the exfoliative cells of cervical cancer
Tong Ren, Jing Suo, Shikai Liu, Shu Wang, Shan Shu, Yang Xiang, Jing-He Lang
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| 5 |
Chromosomal Microarray With Clinical Diagnostic Utility in Children With Developmental Delay or Intellectual Disability
Jin Sook Lee, Hee Hwang, Soo Yeon Kim, Ki Joong Kim, Jin Sun Choi, Mi Jung Woo, Young Min Choi, Jong Kwan Jun, Byung Chan Lim, Jong-Hee Chae
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| 6 |
Copy Number Profiling of MammaPrint™ Genes Reveals Association with the Prognosis of Breast Cancer Patients
Areej Fatima, Fomaz Tariq, Muhammad Faraz Arshad Malik, Muhammad Qasim, Farhan Haq
J Breast Cancer.2017;20(3):246-253. Published online 2017 September 22
DOI: http://dx.doi.org/10.4048/jbc.2017.20.3.246
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| 7 |
Routine Chromosomal Microarray Analysis is Necessary in Korean Patients With Unexplained Developmental Delay/Mental Retardation/Autism Spectrum Disorder
Saeam Shin, Nae Yu, Jong Rak Choi, Seri Jeong, Kyung-A Lee
Ann Lab Med.2015;35(5):510-518. Published online 2015 July 15
DOI: http://dx.doi.org/10.3343/alm.2015.35.5.510
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| 8 |
Copy Number Variation Burden on Asthma Subgenome in Normal Cohorts Identifies Susceptibility Markers
Sangeetha Vishweswaraiah, Avinash M Veerappa, Padukudru A Mahesh, Sareh R Jahromi, Nallur B. Ramachandra
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| 9 |
Clinical Significance of Previously Cryptic Copy Number Alterations and Loss of Heterozygosity in Pediatric Acute Myeloid Leukemia and Myelodysplastic Syndrome Determined Using Combined Array Comparative Genomic Hybridization plus Single-Nucleotide Polymorphism Microarray Analyses
Kyung-Nam Koh, Jin Ok Lee, Eul Ju Seo, Seong Wook Lee, Jin Kyung Suh, Ho Joon Im, Jong Jin Seo
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| 10 |
Array-Based Comparative Genomic Hybridization in 190 Korean Patients with Developmental Delay and/or Intellectual Disability: A Single Tertiary Care University Center Study
Cha Gon Lee, Sang-Jin Park, Jun-No Yun, Jung Min Ko, Hyon-Ju Kim, Shin-Young Yim, Young Bae Sohn
Yonsei Med J.2013;54(6):1463-1470. Published online 2013 October 1
DOI: http://dx.doi.org/10.3349/ymj.2013.54.6.1463
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| 11 |
Correlation of DEFA1 Gene Copy Number Variation with Intestinal Involvement in Behcet's Disease
Joong Kyong Ahn, Hoon-Suk Cha, Jaejoon Lee, Chan Hong Jeon, Eun-Mi Koh
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| 12 |
Prognostic significance of syndecan-1 expression in cervical cancers
Yu Im Kim, Ahwon Lee, Bum Hee Lee, Su Young Kim
J Gynecol Oncol.2011;22(3):161-167. Published online 2011 September 28
DOI: http://dx.doi.org/10.3802/jgo.2011.22.3.161
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