Survival in trisomy 18: life tables for use in genetic counselling and clinical paediatrics. Clin Genet 1985; 27: 59-61.Carter P , Pearn J , Bell J , Martin N , Anderson N. 1985 . Survival in trisomy 18 . Clin Genet 27 : 59 – 61 ....
Rates and survival figures for trisomy 13 and trisomy 18 have been calculated for Denmark (DK) based on a 10-year period (1977–86). The data have been ascertained through The Danish Central Cytogenetic Register, all cytogenetic laboratories in DK, paediatric departments throughout the country, ...
Trisomy 13 (T13) and trisomy 18 (T18) are among the most prevalent autosomal trisomies. Both are associated with a very high risk of mortality. Numerous instances, however, of long-term survival of children with T13 or T18 have prompted some clinicians to pursue aggressive treatment instead ...
Moreover, an increase in the number of 7q signals, often accompanied by trisomy 8, has been associated with disease progression. The gene expression profile of HSTL appears distinct from other types of PTCL and is characterized by overexpression of NK cell-associated molecules such as killer ...
sclerosis69and Down syndrome (trisomy 21)70with log2-fold changes of −1.5 and −2.9, respectively, compared with those in normal cells. IGF2-AS expression was up-regulated in glioblastoma71with a log2-fold change of 3 and in childhood brain tumour ependymoma62with a log2-fold change ...
Antonio Cuneo, Renato Bigoni, Massimo Balboni, Maria Gretel Carli, Nadia Piva, Franca Fagioli, Angela Latorraca, Iwona Wlodarska, Herman Van Den Berghe & Gianluigi Castoldi. (1994)Trisomy 12 in Chronic Lymphocytic Leukemia and Hairy Cell Leukemia: A Cytogenetic and Interphase Cytogenetic Study.Leuk...
Moran, in an excellent review [9], defined idiopathic infantile arterial calcification as a rare disorder of undetermined etiology, characterized by deposition of calcific material along the internal elastic membrane of large, medium, and small arteries. Fibrous proliferation in the intima occurs and ...
In addition, VH usage and trisomy 12 were associated with TFS for men and women, respectively. Kaplan-Meier survival curves were used to estimate TFS and the log-rank test to compare survival curves. A value of P < 0.05 was considered statistically significant. All analyses were performed ...
33 Mutational fre- quency of IDH1 in primary AML is B9% and the mutations usually cluster with normal karyotype, although a possible association with trisomy 8 has been suggested.24 More recently, IDH2 mutations were also reported in primary AML.32,33 IDH 6 List A, Dewald G, Bennett J,...
Outcome of patients with trisomy 8 is poor in the absence of t(8;21), inv(16)/t(16;16), and t(9;11) Trisomy 8 is the most common trisomy in de novo AML (Table 3). However, the +8 group is heterogeneous, because +8 can be the sole abnormality detected, can be part of a ...