|1.||Lennarts, Melanie: 1 article (08/2010)|
|2.||Stevens, Servi J C: 1 article (08/2010)|
|3.||Breukels, Mijke A: 1 article (08/2010)|
|4.||Traa, Erik: 1 article (08/2010)|
|5.||Droog, Richard P: 1 article (08/2010)|
|6.||Rauh-van Delst, Marion: 1 article (08/2010)|
|7.||Smeets, Eric E J G L: 1 article (08/2010)|
|8.||van den Broek, Naomi: 1 article (08/2010)|
|9.||Engelen, John J M: 1 article (08/2010)|
|10.||Janssen, Jannie W H: 1 article (08/2010)|
08/19/1992 - "They maintained a near-diploid karyotype with few chromosomal markers such as trisomy 1q (S1T3) and trisomy 8q (S2T2), which are most common in breast cancer in vivo. "
11/15/1996 - "Five additional cases of trisomy 8q, 3 more cases of trisomy 11q, and 2 more cases of trisomies 21q and 22q were shown by FISH. "
08/01/2006 - "Trisomy 8q and partial trisomy 22 in a 43-year-old man with moderate intellectual disability, epilepsy and large cell non-Hodgkin lymphoma."
|2.||T-Cell Prolymphocytic Leukemia (Leukemia, T Cell, Chronic)
10/01/1998 - "14q11 abnormality and trisomy 8q are not common in Japanese T-cell prolymphocytic leukemia."
01/15/1994 - "Clones with both inv(14)(q11q32.1) and trisomy 8q, mostly caused by i(8q)(q10), were found in all cases of T-cell chronic lymphocytic leukemia (T-CLL) and T-cell prolymphocytic leukemia (T-PLL). "
02/01/1993 - "Consistent occurrence of monosomy 3 and trisomy 8q."
01/15/1994 - "On the contrary, T-CLL, T-PLL, and cutaneous T-cell lymphomas (CTCL) showed complex clones (P < .0001), duplications in 6p (P < .01), deletions in 6q (P < .01), trisomy 8q (P < .00001), inv(14) (P < .00001), and monosomy 13 or changes of 13q14 (P < .001) more frequently than the other low-grade PTL. "
02/01/1993 - "The tumors previously exposed to radiation were characterized by more complex changes, with monosomy 3 and trisomy 8q detected in three cases each. "
02/01/1993 - "Uveal melanoma is characterized by monosomy 3 and trisomy 8q in most cases. "
|4.||Chromosome Aberrations (Chromosome Abnormalities)
08/01/2006 - "Given that trisomy 8q is the most frequent secondary chromosomal abnormality in hematological diseases, the possibility of a genetic predisposition for these disorders in patients with 8q duplication is raised."
11/01/1994 - "Recurrent numerical chromosome aberrations comprised -X, -Y, -13, +X, +3, +5 and +7. Recurrent structural aberrations included t/del(1)(p31-32), t(2;5)(p23;q35), dup(5)(q23q31-32), t/dup(6q), t/del(6q), trisomy 7q, and trisomy 8q, mostly due to i(8)(q10), and changes in 14q11 and 14q32.1, mostly due to inv(14)(q11q32.1), t/del(13)(q14), t(6;7)(q13;q13), and t(13;17)(q11-13;p11). "
|5.||Genetic Predisposition to Disease (Genetic Predisposition)
|2.||Chromosome 11q trisomy
|3.||trisomy 7q Chromosome 7
|5.||Recombinant chromosome 8 syndrome