Pages that link to "Q40869252"

The following pages link to The most frequent constitutional translocation in humans, the t(11;22)(q23;q11) is due to a highly specific alu-mediated recombination (Q40869252):

Displaying 17 items.

• AT-rich palindromes mediate the constitutional t(11;22) translocation. (Q34043814) (← links)
• The role of Alu repeat clusters as mediators of recurrent chromosomal aberrations in tumors (Q34804028) (← links)
• Inviting instability: Transposable elements, double-strand breaks, and the maintenance of genome integrity. (Q35748440) (← links)
• Mechanisms leading to nonrandom, nonhomologous chromosomal translocations in leukemia (Q36677854) (← links)
• The impact of transposable elements in environmental adaptation. (Q38072072) (← links)
• Large duplications at reciprocal translocation breakpoints that might be the counterpart of large deletions and could arise from stalled replication bubbles (Q38440779) (← links)
• Human embryonic stem cells carrying an unbalanced translocation demonstrate impaired differentiation into trophoblasts: an in vitro model of human implantation failure (Q38940959) (← links)
• Organization and evolution of a gene-rich region of the mouse genome: a 12.7-Mb region deleted in the Del(13)Svea36H mouse (Q40254032) (← links)
• Constitutional chromosome aberrations as pathogenetic events in hematologic malignancies. (Q45991378) (← links)
• Bioinformatics and genomic analysis of transposable elements in eukaryotic genomes (Q46681274) (← links)
• Recent evolution of the human pathogen Cryptococcus neoformans by intervarietal transfer of a 14-gene fragment (Q47194021) (← links)
• Comparative analysis of the bovine MHC class IIb sequence identifies inversion breakpoints and three unexpected genes (Q48094509) (← links)
• High incidence of familial breast cancer segregates with constitutional t(11;22)(q23;q11). (Q48469722) (← links)
• Cri du chat syndrome after preimplantation genetic diagnosis for reciprocal translocation (Q51032067) (← links)
• Characterisation of a non-recurrent familial translocation t(7;9)(q11.23;p24.3) points to a recurrent involvement of the Williams–Beuren syndrome region in chromosomal rearrangements (Q61983612) (← links)
• Mortality and cancer incidence in carriers of constitutional t(11;22)(q23;q11) translocations: A prospective study (Q62583498) (← links)
• Molecular cytogenetic analysis of breast cancer: a combined multicolor fluorescence in situ hybridization and G-banding study of uncultured tumor cells (Q79974782) (← links)