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Nature Communications|March 14, 2013
Two sequential cleavage reactions on cruciform DNA structures cause palindrome-mediated chromosomal translocationsHidehito Inagaki, Tamae Ohye, Hiroshi Kogo, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 5, 2008
Evaluation of potential modifiers of the cardiac phenotype in the 22q11.2 deletion syndromeElizabeth Goldmuntz, Deborah A Driscoll, Beverly S Emanuel, et al.
Human Mutation|August 24, 2005
Palindromic AT-rich repeat in the NF1 gene is hypervariable in humans and evolutionarily conserved in primatesHidehito Inagaki, Tamae Ohye, Hiroshi Kogo, et al.
American Journal of Medical Genetics. Part A|August 6, 2003
Myoclonus in a patient with a deletion of the epsilon-sarcoglycan locus on chromosome 7q21Ralph J DeBerardinis, Danielle Conforto, Karen Russell, et al.
American Journal of Medical Genetics. Part A|April 5, 2014
Further phenotype description, genotype characterization in patients with de novo interstitial deletion on 2p23.2-24.1Mercedes Bloch, Anissa Leonard, Andreas A Diplas, et al.
Molecular Cytogenetics|September 9, 2011
DNA secondary structure is influenced by genetic variation and alters susceptibility to de novo translocationTakema Kato, Hidehito Inagaki, Maoqing Tong, et al.
Pediatric Cardiology|April 23, 2013
22q11.2 deletions in patients with conotruncal defects: data from 1,610 consecutive casesShabnam Peyvandi, Philip J Lupo, Jennifer Garbarini, et al.
American Journal of Medical Genetics. Part A|August 7, 2007
Primary amenorrhea and absent uterus in the 22q11.2 deletion syndromeUsha T Sundaram, Donna M McDonald-McGinn, Dale Huff, et al.
Genes|September 23, 2022
A Novel Non-Allelic Homologous Recombination Event in a Parent with an 11;22 Reciprocal Translocation Leading to 22q11.2 Deletion SyndromeSteven Pastor, Oanh Tran, Daniel E McGinn, et al.
American Journal of Human Genetics|August 16, 2006
Meiotic recombination and spatial proximity in the etiology of the recurrent t(11;22)Terry Ashley, Ann P Gaeth, Hidehito Inagaki, et al.
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