Chromosome painting using FISH (fluorescence in situ hybridization) with chromosome-6-specific library demonstrates the origin of a de novo 6q+ marker chromosome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1993.tb03809.x/fullpdf
Reference16 articles.
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2. Molecular identification of a small supernumerary marker chromosome by in situ hybridization: diagnosis of an isochromosome 18p with probe L1.84;Blennow;Clin Genet,1991
3. Chromosomal origin of small ring marker chromosomes in man: characterization by molecular genetics;Callen;Am J Hum Genet,1991
4. Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics;Carter;J Med Genet,1992
5. Duplication 6q24-6qter in an infant from a balanced paternal translocation;Chase;Am J Med Genet,1983
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2. Molecular characterization of a de novo 6q24.2q25.3 duplication interrupting UTRN in a patient with arthrogryposis;American Journal of Medical Genetics Part A;2010-06-25
3. A 15Mb duplication of 6q24.1–q25.3 associated with typical but milder features of the duplication 6q syndrome;European Journal of Medical Genetics;2008-07
4. Prenatal diagnosis of a de novo trisomy 6q22.2→6qter and monosomy lpter→1p36.3. Case report with a 2-year follow-up and a brief review of other prenatal cases of partial trisomy 6q;Clinical Genetics;2008-06-28
5. A de novo 6q11-q15 duplication investigated by chromosome painting;Clinical Genetics;2008-06-28
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