Involvement of a palindromic chromosome 22-specific low-copy repeat in a constitutional t(X; 22)(q27;q11)
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.2002.620510.x/fullpdf
Reference33 articles.
1. Segmental duplications. an'expanding′ role in genomic instability and disease;Emanuel;Nat Rev Genet,2001
2. Regions of genomic instability on 22q11 and 11q23 as the etiology for the recurrent constitutional t(11;22);Kurahashi;Hum Mol Genet,2000
3. Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22);Kurahashi;Am J Hum Genet,2000
4. Clustered 11q23 and 22q11 breakpoints and 3:1 meiotic malsegregation in multiple unrelated t(11;22) families;Shaikh;Am J Hum Genet,1999
5. AT-rich palindromes mediate the constitutional t(11;22) translocation;Edelmann;Am J Hum Genet,2001
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3. Palindrome Mediated Translocation in Human: Where Do We Go from Here?;International Journal of Neuroscience and Research;2017-08-16
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