Cryptic Translocation Identification in Human and Mouse Using Several Telomeric Multiplex FISH (TM-FISH) Strategies-Reference-Cited by-同舟云学术

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Cryptic Translocation Identification in Human and Mouse Using Several Telomeric Multiplex FISH (TM-FISH) Strategies

Published:2001-04 Issue:4 Volume:81 Page:483-491
ISSN:0023-6837
Container-title:Laboratory Investigation
language:en
Short-container-title:Lab Invest

Author:

Henegariu Octavian,Artan Sevilhan,Greally John M,Chen Xiao-Ning,Korenberg Julie R,Vance Gail H,Stubbs Lisa,Bray-Ward Patricia,Ward David C

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Molecular Biology,Pathology and Forensic Medicine

Link

http://www.nature.com/articles/3780256.pdf

Reference19 articles.

1. Azofeifa J, Fauth C, Kraus J, Maierhofer C, Langer S, Bolzer A, Reichman J, Schuffenhauer S, and Speicher MR (2000). An optimized probe set for the detection of small interchromosomal aberrations by use of 24-color FISH. Am J Hum Genet 66: 1684–1688.

2. Bacino CA, Kashork CD, Davino NA, and Shaffer LG (2000). Detection of a cryptic translocation in a family with mental retardation using FISH and telomere region-specific probes. Am J Med Genet 92: 250–255.

3. Ballif BC, Kashork CD, and Shaffer LG (2000). FISHing for mechanisms of cytogenetically defined terminal deletions using chromosome-specific subtelomeric probes [In Process Citation]. Eur J Hum Genet 8: 764–770.

4. Flint J, Wilkie AO, Buckle VJ, Winter RM, Holland AJ, and McDermid HE (1995). The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation. Nat Genet 9: 132–140.

5. Ghaffari SR, Boyd E, Tolmie JL, Crow YJ, Trainer AH, and Connor JM (1998). A new strategy for cryptic telomeric translocation screening in patients with idiopathic mental retardation. J Med Genet 35: 225–233.

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