Microarray-based Comparative Genomic Hybridization (aCGH) (2024)

Albertson, D. G., et al. Quantitative mapping of amplicon structure by array CGH identifies CYP24 as a candidate oncogene. Nature Genetics 25, 144–146 (2000) doi:10.1038/75985 (link to article)

Ballif, B. C., et al. Monosomy 1p36 breakpoint junctions suggest pre-meiotic breakage-fusion-bridge cycles are involved in generating terminal deletions. Human Molecular Genetics 12, 2153–2165 (2003) doi:10.1093/hmg/ddg231 (link to article)

———. Translocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(1;1)(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangements. Human Genetics 114, 198–206 (2004) doi:10.1007/s00439-003-1029-y

———. Discovery of a previously unrecognized microdeletion syndrome of 16p11.2-p12.2. Nature Genetics 39, 1071–1073 (2007a) (link to article)

———. The clinical utility of enhanced subtelomeric coverage in array CGH. American Journal of Medical Genetics 143A, 1850–1857 (2007b) doi:10.1002/ajmg.a.31842

———. Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication. Molecular Cytogenetics 1, 1–7 (2008a) doi:10.1186/1755-8166-1-8

———. Identification of a previously unrecognized microdeletion syndrome of 16q11.2q12.2. Clinical Genetics (in press) (2008b) doi:10.1111/j.1399-0004.2008.01094.x

Barber, J. C. K., et al. 8p23.1 duplication syndrome: A novel genomic condition with unexpected complexity revealed by array CGH. European Journal of Human Genetics 16, 18–27 (2008) doi:10.1038/sj.ejhg.5201932 (link to article)

Berg, J. S., et al. Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region. Genetics in Medicine 9(7), 427–441 (2007)

Biesecker, L. G. The end of the beginning of chromosome ends. American Journal of Medical Genetics 107, 263–266 (2002) doi:10.1002/ajmg.10160

Borozdin, W., et al. Detection of heterozygous SALL1 deletions by quantitative real time PCR proves the contribution of a SALL1 dosage effect in the pathogenesis of Townes-Brocks syndrome. Human Mutation 27, 211–212 (2006) doi:10.1002/humu.9396 (link to article)

Brewer, C., et al. A chromosomal deletion map of human malformations. American Journal of Human Genetics 63, 1153–1159 (1998)

del Gaudio, D., et al. Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males. Genetics in Medicine 8, 784–792 (2006)

DeRisi, J., et al. Use of a cDNA microarray to analyse gene expression patterns in human cancer. Nature Genetics 14, 457–460 (1996) doi:10.1038/ng1296-457 (link to article)

de Vries, B. B. A., et al. Diagnostic genome profiling in mental retardation. American Journal of Human Genetics 77, 606–616 (2005)

Ensenauer, R. E., et al. Microduplication 22q11.2, an emerging syndrome: Clinical, cytogenetic, and molecular analysis of thirteen patients. American Journal of Human Genetics 73, 1027–1040 (2003)

Flint, J., et al. The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation. Nature Genetics 9, 132–140 (1995) doi:10.1038/ng0295–132 (link to article)

Hassed, S. J., et al. A new genomic duplication syndrome complementary to the velocardiofacial (22q11 deletion) syndrome. Clinical Genetics 65, 400–404 (2004) doi:10.1111/j.0009-9163.2004.0212.x

Kallioniemi, A., et al. Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors. Science 258, 818–821 (1992) doi:10.1126/science.1359641

Kirchhoff, M., et al. Detection of chromosomal gains and losses in comparative genomic hybridization analysis based on standard reference intervals. Cytometry 31, 163–173 (1998)

———. High resolution comparative genomic hybridisation in clinical cytogenetics. Journal of Medical Genetics 38, 740–744 (2001) doi:10.1136/jmg.38.11.740

Knight, S. J., et al. Subtle chromosomal rearrangements in children with unexplained mental retardation. Lancet 354, 1676–1681 (1999)

Kriek, M., et al. Copy number variation in regions flanked (or unflanked) by duplicons among patients with developmental delay and/or congenital malformations; detection of reciprocal and partial Williams-Beuren duplications. European Journal of Human Genetics 14, 180–189 (2006) doi:10.1038/sj.ejhg.5201540 (link to article)

Lichter, P., et al. Comparative genomic hybridization: Uses and limitations. Seminars in Hematology 37, 348–357 (2000)

Lu, X., et al. Clinical implementation of chromosomal microarray analysis: Summary of 2513 postnatal cases. PLoS ONE 2, e327 (2007) doi:10.1371/journal.pone.0000327

Lucito, R., et al. Representational oligonucleotide microarray analysis: A high-resolution method to detect genome copy number variation. Genome Research 13, 2291–2305 (2003)

Lupski, J. R. Genomic disorders: Structural features of the genome can lead to DNA rearrangements and human disease traits. Trends in Genetics 14, 417–422 (1998) doi:10.1016/S0168-9525(98)01555-8

Pinkel, D., et al. High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays. Nature Genetics 20, 207–211 (1998) doi:10.1038/2524 (link to article)

Potocki, L., et al. Molecular mechanism for duplication 17p11.2—The hom*ologous recombination reciprocal of the Smith-Magenis microdeletion. Nature Genetics 24, 84–87 (2000) doi:10.1038/71743 (link to article)

———. Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype. American Journal of Human Genetics 80, 633–649 (2007)

Ravnan, J. B., et al. Subtelomere FISH analysis of 11,688 cases: An evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities. Journal of Medical Genetics 43, 478–489 (2006) doi:10.1136/jmg.2005.036350

Saccone, S., et al. The highest gene concentrations in the human genome are in telomeric bands of metaphase chromosomes. Proceedings of the National Academy of Sciences 89, 4913–4917 (1992)

Schena, M., et al. Quantitative monitoring of gene expression patterns with a complementary DNA microarray. Science 270, 467–470 (1995) doi:10.1126/science.270.5235.467

Shaffer, L. G., & Lupski, J. R. Molecular mechanisms for constitutional chromosomal rearrangements in humans. Annual Review of Genetics 34, 297–329 (2000)

Shaffer, L. G., et al. Diagnosis of CMT1A duplications and HNPP deletions by interphase FISH: Implications for testing in the cytogenetics laboratory. American Journal of Medical Genetics 69, 325–331 (1997)

———. Molecular cytogenetics of contiguous gene syndromes: Mechanisms and consequences of gene dosage imbalance. In Metabolic and Molecular Basis of Inherited Disease, 8th ed., ed. C. R. Scriver, et al. (New York, McGraw Hill, 2001), vol. 1, p. 1291.

———. The identification of microdeletion syndromes and other chromosome abnormalities: Cytogenetic methods of the past, new technologies for the future. American Journal of Medical Genetics 145C, 335–345 (2007) doi:10.1002/ajmg.c.30152

Shaw-Smith, C., et al. Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features. Journal of Medical Genetics 41, 241–248 (2004) doi:10.1136/jmg.2003.017731

She, X., et al. The structure and evolution of centromeric transition regions within the human genome. Nature 430, 857–864 (2004) doi:10.1038/nature02806 (link to article)

Solinas-Toldo, S., et al. Matrix-based comparative genomic hybridization: Biochips to screen for genomic imbalances. Genes, Chromosomes, and Cancer 20, 399–407 (1997)

Somerville, M. J., et al. Severe expressive-language delay related to duplication of the Williams-Beuren locus. New England Journal of Medicine 353, 1694–1701 (2005)

Speicher, M. R., et al. Molecular cytogenetic analysis of formalin-fixed, paraffin-embedded solid tumors by comparative genomic hybridization after universal DNA-amplification Human Molecular Genetics 2, 1907–1914 (1993)

Vissers, L. E., et al. Array-based comparative genomic hybridization for the genome-wide detection of submicroscopic chromosomal abnormalities. American Journal of Human Genetics 73, 1261–1270 (2003)

Yobb, T. M., et al. Microduplication and triplication of 22q11.2: A highly variable syndrome. American Journal of Human Genetics 76, 865–876 (2005)

Microarray-based Comparative Genomic Hybridization (aCGH) (2024)

References

Top Articles
Target to Set New Starting Wage Range and Expand Access to Health Care Benefits to More Team Members
Export | Cars-4Sale.nl
Spasa Parish
Rentals for rent in Maastricht
159R Bus Schedule Pdf
Sallisaw Bin Store
Black Adam Showtimes Near Maya Cinemas Delano
Espn Transfer Portal Basketball
Pollen Levels Richmond
11 Best Sites Like The Chive For Funny Pictures and Memes
Things to do in Wichita Falls on weekends 12-15 September
Craigslist Pets Huntsville Alabama
Paulette Goddard | American Actress, Modern Times, Charlie Chaplin
What's the Difference Between Halal and Haram Meat & Food?
R/Skinwalker
Rugged Gentleman Barber Shop Martinsburg Wv
Jennifer Lenzini Leaving Ktiv
Justified - Streams, Episodenguide und News zur Serie
Epay. Medstarhealth.org
Olde Kegg Bar & Grill Portage Menu
Cubilabras
Half Inning In Which The Home Team Bats Crossword
Amazing Lash Bay Colony
Juego Friv Poki
Dirt Devil Ud70181 Parts Diagram
Truist Bank Open Saturday
Water Leaks in Your Car When It Rains? Common Causes & Fixes
What’s Closing at Disney World? A Complete Guide
New from Simply So Good - Cherry Apricot Slab Pie
Drys Pharmacy
Ohio State Football Wiki
Find Words Containing Specific Letters | WordFinder®
Abby's Caribbean Cafe
Joanna Gaines Reveals Who Bought the 'Fixer Upper' Lake House and Her Favorite Features of the Milestone Project
Tri-State Dog Racing Results
Navy Qrs Supervisor Answers
Trade Chart Dave Richard
Lincoln Financial Field Section 110
Free Stuff Craigslist Roanoke Va
Stellaris Resolution
Wi Dept Of Regulation & Licensing
Pick N Pull Near Me [Locator Map + Guide + FAQ]
Crystal Westbrooks Nipple
Ice Hockey Dboard
Über 60 Prozent Rabatt auf E-Bikes: Aldi reduziert sämtliche Pedelecs stark im Preis - nur noch für kurze Zeit
Wie blocke ich einen Bot aus Boardman/USA - sellerforum.de
Infinity Pool Showtimes Near Maya Cinemas Bakersfield
Dermpathdiagnostics Com Pay Invoice
How To Use Price Chopper Points At Quiktrip
Maria Butina Bikini
Busted Newspaper Zapata Tx
Latest Posts
Article information

Author: Ouida Strosin DO

Last Updated:

Views: 5456

Rating: 4.6 / 5 (76 voted)

Reviews: 91% of readers found this page helpful

Author information

Name: Ouida Strosin DO

Birthday: 1995-04-27

Address: Suite 927 930 Kilback Radial, Candidaville, TN 87795

Phone: +8561498978366

Job: Legacy Manufacturing Specialist

Hobby: Singing, Mountain biking, Water sports, Water sports, Taxidermy, Polo, Pet

Introduction: My name is Ouida Strosin DO, I am a precious, combative, spotless, modern, spotless, beautiful, precious person who loves writing and wants to share my knowledge and understanding with you.