نتایج جستجو برای: ellis

تعداد نتایج: 4036  

Journal: :Math. Log. Q. 2015
Grzegorz Jagiella

We investigate definable topological dynamics of groups definable in an o-minimal expansion of the field of reals. Assuming that a definable group G admits a model-theoretic analogue of Iwasawa decomposition, namely the compact-torsion-free decomposition G KH, we give a description of minimal subflows and the Ellis group of its universal definable flow SGpRq in terms of this decomposition. In p...

Journal: :Pediatric dentistry 2004
Abel Cahuana Camila Palma Wilber Gonzáles Esther Geán

Ellis-van Creveld syndrome, or chondroectodermal dysplasia, is an autosomal recessive disorder with characteristic clinical manifestations. Its incidence in the general population is low. The oral manifestations of Ellis-van Creveld are found in soft tissues and teeth, but the dental literature on the subject is scarce. In the last 20 years, 5 cases of Ellis-van Creveld syndrome have been follo...

1978
Subash Singh Vandana Arya M Jonathan Daniel Vijeev Vasudevan

Ellis-van Creveld syndrome also known as chondroectodermal dysplasia or mesoectodermal dysplasia; a rare genetic disorder of the skeletal dysplasia. 'Six-fingered dwarfism' (digital integer deficiency) was an alternative designation used for this condition when it was being studied in the Amish. It is characterized by short-limb dwarfism, polydactyly, malformation of the bones of the wrist, dys...

1996
Andreas Schäfer

The effect from quark masses and transversal motion on the Gottfried, Bjorken, and Ellis-Jaffe sum rules is examined by using a quark-parton model of nucleon structure functions based on an improved scaling variable. Its use results in corrections to the Gottfried, Bjorken, and Ellis-Jaffe sum rules. We use the Brodsky-Huang-Lepage prescription of light-cone wavefunctions to estimate the size o...

ALI ANDON PETROSSIANS, MAJID MALEKI,

Ellis-van Creveld syndrome is transmitted as an autosomal recessive trait. This syndrome is accompanied in 60% of cases with congenital heart disease, mostly single atrium or large ASD. Patients are mostly symptomatic, but in this rare case despite 68 years of age, the patient was free of symptoms except for complete heart block for which pacemaker was inserted

2008
A. Ellis G. Zarris D. Simeonidou J. Leuthold D. Cotter

We present the first experimental demonstration of an asynchronous digital optical regenerator at 42.67 Gbit/s. The system effectively retimes incoming asynchronous data bursts to a local clock without burst mode clock recovery and converts the signal to a desired wavelength and duty cycle. ©2008 Optical Society of America OCIS codes: (060.2330) Fiber optics communications; (060.4510) Optical c...

Journal: :Classical and Quantum Gravity 2005

Journal: :Journal of Evolution of Medical and Dental Sciences 2014

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