scholarly journals Classification of normal congruence subgroups of $G \left( {\sqrt q } \right)$, II

1988 ◽  
Vol 64 (6) ◽  
pp. 205-207
Author(s):  
Toshikazu Takagi
2008 ◽  
Vol 15 (04) ◽  
pp. 707-720
Author(s):  
Bo Chen ◽  
Pingzhi Yuan

Hecke groups are an important class of discrete subgroups of PSL(2, ℝ), which play an important role in the study of Dirichlet series. Subgroups with finite index of a Hecke group, which are called congruence subgroups, are often used. Let q be a positive integer with [Formula: see text]. For the Hecke group [Formula: see text], the structures of principal congruence subgroups and normal congruence subgroups of level m are investigated in many papers, where m is a prime or a power of an odd prime. In this paper, we deal with the case that the level m is a power of 2.


1966 ◽  
Vol 24 ◽  
pp. 21-23
Author(s):  
Y. Fujita

We have investigated the spectrograms (dispersion: 8Å/mm) in the photographic infrared region fromλ7500 toλ9000 of some carbon stars obtained by the coudé spectrograph of the 74-inch reflector attached to the Okayama Astrophysical Observatory. The names of the stars investigated are listed in Table 1.


Author(s):  
Gerald Fine ◽  
Azorides R. Morales

For years the separation of carcinoma and sarcoma and the subclassification of sarcomas has been based on the appearance of the tumor cells and their microscopic growth pattern and information derived from certain histochemical and special stains. Although this method of study has produced good agreement among pathologists in the separation of carcinoma from sarcoma, it has given less uniform results in the subclassification of sarcomas. There remain examples of neoplasms of different histogenesis, the classification of which is questionable because of similar cytologic and growth patterns at the light microscopic level; i.e. amelanotic melanoma versus carcinoma and occasionally sarcoma, sarcomas with an epithelial pattern of growth simulating carcinoma, histologically similar mesenchymal tumors of different histogenesis (histiocytoma versus rhabdomyosarcoma, lytic osteogenic sarcoma versus rhabdomyosarcoma), and myxomatous mesenchymal tumors of diverse histogenesis (myxoid rhabdo and liposarcomas, cardiac myxoma, myxoid neurofibroma, etc.)


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