Overview of Cytogenetic Technologies

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참고문헌 (53)

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23. Bejjani BA, "Clinical utility of contemporary molecular cytogenetics", Annu Rev Genomics Hum Genet, 9, pp.71~86 (2008)
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25. Marilyn M. Li, "Clinical Application of Microarray-Based Molecular Cytogenetics: An Emerging New Era of Genomic Medicine", The Journal of Pediatrics, 155(3), pp.311~317 (2009), Elsevier BV[DOI]
26. L.G. Shaffer, "Medical applications of array CGH and the transformation of clinical cytogenetics", Cytogenetic and Genome Research, 115(3-4), pp.303~309 (2006), S. Karger AG[DOI]
27. Ji Un Kang, "High Frequency of Genetic Alterations in Non-small Cell Lung CancerDetected by Multi-target Fluorescence In Situ Hybridization", Journal of Korean Medical Science, 22(S), pp.47~51 (2007), 대한의학회
28. A. M. Mohamed, "Cytogenomic characterization of 1q43q44 deletion associated with 4q32.1q35.2 duplication and phenotype correlation", Molecular Cytogenetics, 11(1), pp.57~ (2018), Springer Nature[DOI]
29. Ramachandran Krishna Chandran, "Genomic amplification of BCR-ABL1 fusion gene and its impact on the disease progression mechanism in patients with chronic myelogenous leukemia", Gene, 686, pp.85~91 (2019), Elsevier BV[DOI]
30. F. Steffen Krause, "Clinical decisions for treatment of different staged bladder cancer based on multitarget fluorescence in situ hybridization assays?", World Journal of Urology, 24(4), pp.418~422 (2006), Springer Nature[DOI]
31. Gullotta F, "Prenatal diagnosis of genomic disorders and chromosome abnormalities using array-based comparative genomic hybridization", J Prenat Med, 1, pp.16~22 (2007)
32. Melissa S Savage, "Evolving applications of microarray analysis in prenatal diagnosis", Current Opinion in Obstetrics and Gynecology, 23(2), pp.103~108 (2011), Ovid Technologies (Wolters Kluwer Health)[DOI]
33. David Gresham, "Comparing whole genomes using DNA microarrays", Nature Reviews Genetics, 9(4), pp.291~302 (2008), Springer Nature[DOI]
34. Jiun Kang, "Clinical Implications of Microarray in Cancer Medicine", International Journal of Cancer Research, 11(4), pp.150~158 (2015), Science Alert[DOI]
35. Wilch ES, "Historical and clinical perspectives on chromosomal translocations", Adv Exp Med Biol, 1044, pp.1~14 (2018)[DOI]
36. Lin SY, "Application of molecular cytogenetic techniques to characterize the aberrant Y chromosome arising de novo in a male fetus with mosaic 45,X and solve the discrepancy between karyotyping, chromosome microarray, and multiplex ligation dependent probe amplification", J Formos Med Assoc, 117, pp.1027~1031 (2018)
37. John C. Herriges, "Identification of two 14q32 deletions involving DICER1 associated with the development of DICER1-related tumors", European Journal of Medical Genetics, 62(1), pp.9~14 (2018), Elsevier BV[DOI]
38. Irene Plaza Pinto, "Mosaic Tetrasomy of 9p24.3q21.11 postnatally identified in an infant born with multiple congenital malformations: a case report", BMC Pediatrics, 18(1), pp.298~ (2018), Springer Nature[DOI]
39. Milton Rego de Paula Junior, "High Frequency of Copy-Neutral Loss of Heterozygosity in Patients with Myelofibrosis", Cytogenetic and Genome Research, 154(2), pp.62~70 (2018), S. Karger AG[DOI]
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41. Bert B.A. de Vries, "Diagnostic Genome Profiling in Mental Retardation", The American Journal of Human Genetics, 77(4), pp.606~616 (2005), Elsevier BV[DOI]
42. Lisenka E.L.M. Vissers, "Array-Based Comparative Genomic Hybridization for the Genomewide Detection of Submicroscopic Chromosomal Abnormalities", The American Journal of Human Genetics, 73(6), pp.1261~1270 (2003), Elsevier BV[DOI]
43. Gurdeep S Sagoo, "Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13,926 subjects", Genetics in Medicine, 11(3), pp.139~146 (2009), Springer Nature[DOI]
44. Ron Hochstenbach, "Array analysis and karyotyping: Workflow consequences based on a retrospective study of 36,325 patients with idiopathic developmental delay in the Netherlands", European Journal of Medical Genetics, 52(4), pp.161~169 (2009), Elsevier BV[DOI]
45. David T. Miller, "Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies", The American Journal of Human Genetics, 86(5), pp.749~764 (2010), Elsevier BV[DOI]
46. Ruan Peng, "Fetal right aortic arch: associated anomalies, genetic anomalies with chromosomal microarray analysis, and postnatal outcome", Prenatal Diagnosis, 37(4), pp.329~335 (2017), Wiley[DOI]
47. Melanie Manning, "Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities", Genetics in Medicine, 12(11), pp.742~745 (2010), Springer Nature[DOI]
48. J. B. Moeschler, "Comprehensive Evaluation of the Child With Intellectual Disability or Global Developmental Delays", PEDIATRICS, 134(3), pp.903~918 (2014), American Academy of Pediatrics (AAP)[DOI]
49. K.D. Lichtenbelt, "From Karyotyping to Array-CGH in Prenatal Diagnosis", Cytogenetic and Genome Research, 135(3-4), pp.241~250 (2011), S. Karger AG[DOI]
50. Lisa G. Shaffer, "Comparison of microarray-based detection rates for cytogenetic abnormalities in prenatal and neonatal specimens", Prenatal Diagnosis, 28(9), pp.789~795 (2008), Wiley[DOI]
51. Paola Evangelidou, "Clinical application of whole-genome array CGH during prenatal diagnosis: Study of 25 selected pregnancies with abnormal ultrasound findings or apparently balanced structural aberrations", Molecular Cytogenetics, 3(1), pp.24~ (2010), Springer Nature[DOI]
52. G D'Amours, "Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype", Clinical Genetics, 81(2), pp.128~141 (2012), Wiley[DOI]
53. S. C. Hillman, "Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis", Ultrasound in Obstetrics & Gynecology, 37(1), pp.6~14 (2011), Wiley[DOI]

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