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• W2124352711 abstract "American Journal of Medical Genetics Part AVolume 152A, Issue 1 p. 209-211 Research Letter Chromosome 6 between-arm intrachromosomal insertion with intrasegmental double inversion: A four-break model† Jia-Chi Wang, Corresponding Author Jia-Chi Wang [email protected] Cytogenetics Laboratory, Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, Canada Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, CanadaCytogenetics Laboratory, McMaster University Medical Center, 1200 Main Street W, Room 3N19, Hamilton, Ontario, Canada L8S 4J9.Search for more papers by this authorLinda Dang, Linda Dang Cytogenetics Laboratory, Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, CanadaSearch for more papers by this authorThomas Fisker, Thomas Fisker Cytogenetics Laboratory, Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, CanadaSearch for more papers by this author Jia-Chi Wang, Corresponding Author Jia-Chi Wang [email protected] Cytogenetics Laboratory, Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, Canada Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, CanadaCytogenetics Laboratory, McMaster University Medical Center, 1200 Main Street W, Room 3N19, Hamilton, Ontario, Canada L8S 4J9.Search for more papers by this authorLinda Dang, Linda Dang Cytogenetics Laboratory, Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, CanadaSearch for more papers by this authorThomas Fisker, Thomas Fisker Cytogenetics Laboratory, Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, CanadaSearch for more papers by this author First published: 23 December 2009 https://doi.org/10.1002/ajmg.a.33161Citations: 4 † How to cite this article: Wang J-C, Dang L, Fisker T. 2010. Chromosome 6 between-arm intrachromosomal insertion with intrasegmental double inversion: a four-break model. Am J Med Genet Part A 152A:209–211. Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL REFERENCES Ardalan A, Prieur M, Choiset A, Turleau C, Goutieres F, Girard-Orgeolet S. 2005. Intrachromosomal insertion mimicking a pericentric inversion: Molecular cytogenetic characterization of a three break rearrangement of chromosome 20. Am J Med Genet Part A 138A: 288– 293. Farrell SA, Chow G. 1992. Intrachromosomal insertion of chromosome 7. Clin Genet 41: 299– 302. Kent WJ, Sugnet CW, Furey TS, Roskin KM, Pringle TH, Zahler AM, Haussler D. 2002. The human genome browser at UCSC. Genome Res 12: 996– 1006. Madan K. 1995. Paracentric inversions: A review. Hum Genet 96: 503– 515. Madan K, Menko FH. 1992. Intrachromosomal insertions: A case report and a review. Hum Genet 89: 1– 9. Madan K, Nieuwint AW. 2002. Reproductive risks for paracentric inversion heterozygotes: Inversion or insertion? That is the question. Am J Med Genet 107: 340– 343. Rose NC, Menacker SJ, Schnur RE, Jackson L, McDonald-McGinn DM, Stump T, Emanuel BS, Zackai EH. 1992. Ocular albinism in a male with del (6)(q13-q15): Candidate region for autosomal recessive ocular albinism? Am J Med Genet 42: 700– 705. South ST, Swensen JJ, Maxwell T, Rope A, Brothman AR, Chen Z. 2006. A new genomic mechanism leading to cri-du-chat syndrome. Am J Med Genet Part A 140A: 2714– 2720. Starke H, Senger G, Kossakiewicz M, Tittelbach H, Rau D, Rubtsov N, Trifonov V, Heller A, Hartmann I, Claussen U, Liehr T. 2001. Maternal insertion of 18q11.2-q12.2 in 18p11.3 of the same chromosome analysed by microdissection and multicolour banding (MCB). Prenat Diagn 21: 1049– 1052. Wang JC, Dang L, Lomax B, Turner L, Shago M, Teebi AS, Klatt R, Macleod PM, Yong SL, Nowaczyk MJ, Eydoux P. 2009. Molecular breakpoint mapping of 6q11-q14 interstitial deletions in seven patients. Am J Med Genet Part A 149A: 372– 379. Citing Literature Volume152A, Issue1January 2010Pages 209-211 ReferencesRelatedInformation" @default.
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