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American Journal of Medical Genetics. Part A|January 19, 2008
Characterization of a cryptic 3.3 Mb deletion in a patient with a "balanced t(15;22) translocation" using high density oligo array CGH and gene expression arraysMarilyn M Li, Manjunath A Nimmakayalu, Danielle Mercer, et al.Human Molecular Genetics|January 11, 2008
Two different forms of palindrome resolution in the human genome: deletion or translocationTakema Kato, Hidehito Inagaki, Hiroshi Kogo, et al.The Journal of Biological Chemistry|June 23, 2004
Cruciform DNA structure underlies the etiology for palindrome-mediated human chromosomal translocationsHiroki Kurahashi, Hidehito Inagaki, Kouji Yamada, et al.Fertility and Sterility|April 24, 2007
Age has no effect on de novo constitutional t(11;22) translocation frequency in spermTakema Kato, Kouji Yamada, Hidehito Inagaki, et al.Human Molecular Genetics|November 14, 2003
A palindrome-mediated mechanism distinguishes translocations involving LCR-B of chromosome 22q11.2Anthony L Gotter, Tamim H Shaikh, Marcia L Budarf, et al.Genome Research|February 3, 2007
Molecular cloning of a translocation breakpoint hotspot in 22q11Hiroki Kurahashi, Hidehito Inagaki, Eriko Hosoba, et al.Cytogenetic and Genome Research|December 20, 2018
The Recurrent t(11;22)(q23;q11.2) Can Occur as a Post-Zygotic EventSarah Correll-Tash, Laura Conlin, Beth A Mininger, et al.American Journal of Medical Genetics. Part A|November 1, 2018
Molecular genetics of 22q11.2 deletion syndromeBernice E Morrow, Donna M McDonald-McGinn, Beverly S Emanuel, et al.American Journal of Medical Genetics. Part A|July 17, 2009
Phenotypic delineation of Emanuel syndrome (supernumerary derivative 22 syndrome): Clinical features of 63 individualsMelissa T Carter, Stephanie A St Pierre, Elaine H Zackai, et al.Pediatrics|December 5, 2003
Chromosome 22q11 deletion in patients with ventricular septal defect: frequency and associated cardiovascular anomaliesDoff B McElhinney, Deborah A Driscoll, Elissa R Levin, et al.Pageof 14