Dual-color fish analysis of breakpoints on robertsonian translocations

Author:

Takahashi Yuri,Fujita Hiroko,Nakamura Yusuke,Kurahashi Hiroki

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical)

Reference19 articles.

1. Antonarakis SE, Adelsberger PA, Petersen MB, Binkert F, Schinzel AA (1990): Analysis of DNA polymorphisms suggests that mostde novo dup(21q) chromosomes in patients with Down syndrome are isochromosomes and not translocations. Am J Hum Genet47: 968–972

2. Brasch JM, Smyth DR (1979): Absence of silver bands in human Robertsonian translocation chromosomes. Cytogenet Cell Genet24: 122–125

3. Cheung SW, Sun L, Featherstone T (1990): Molecular cytogenetic evidence to characterize breakpoint regions in Robertsonian translocations. Cytogenet Cell Genet54: 97–102

4. Earle E, Shaffer LG, Kalitsis P, McQuillan C, Dale S, Choo KHA (1992): Identification of DNA sequences flanking the breakpoint of human t(14q21q) Robertsonian translocations. Am J Hum Genet50: 717–724

5. Grasso M, Giovannucci UML, Tavellini F, Perroni L, Dagna BF (1989): Isochromosome not translocation in trisomy 21q21q. Hum Genet84: 63–65

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