Results 111 to 120 of about 138,756 (354)

The Enumeration of (⊙,∨)-Multiderivations on a Finite MV-Chain

Axioms
In this paper, (⊙,∨)-multiderivations on an MV-algebra A are introduced, the relations between (⊙,∨)-multiderivations and (⊙,∨)-derivations are discussed.
Xueting Zhao, Kai Duo, Aiping Gan, Yichuan Yang   +3 more
doaj   +1 more source

Clinical, Behavioral and Neuroradiological Phenotype in an Italian Cohort of Patients With Xia Gibbs Syndrome: A Multicenter Cross‐Sectional Study and Systematic Literature Review

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Heterozygous variants in the AHDC1 gene are associated with Xia Gibbs Syndrome (XGS), a genetic disorder with a highly variable phenotype. Cognitive impairment, motor delay, language delay, neonatal hypotonia, and sleep apnea are considered “cardinal” signs of the disease.
Giulia Cinelli, Stefania Della Vecchia, Patrizia Bergonzini, Elisa Caramaschi, Elisabetta Spezia, Claudia Parenti, Simona Filomena Madeo, Laura Lucaccioni, Cavalleri Francesca, Marisa Pugliese, Federico Raviglione, Clara Colonna, Olga Calabrese, Ilaria Stanghellini, Maria Carmen Marongiu, Enrico Biagioni, Anna Rita Ferrari, Roberta Battini, Lorenzo Iughetti   +18 more
wiley   +1 more source

(Necessarily) Finite Lexis

Studies in Logic, Grammar and Rhetoric
This short work sets out to argue that the set of simple expressions comprising the lexicon of a given individual and the lexis of a given community are not just contingently but necessarily finite at any given moment in time.
Lemanek Kamil
doaj   +1 more source

Cardinality Networks and Their Applications [PDF]

, 2009
We introduce Cardinality Networks, a new CNF encoding of cardinality constraints. It improves upon the previously existing encodings such as the sorting networks of [ES06] in that it requires much less clauses and auxiliary variables, while arc consistency is still preserved: e.g., for a constraint x 1 + ... + x n  ≤ k, as soon as k variables among
Asín Acha, Roberto Javier, Nieuwenhuis, Robert Lukas Mario, Oliveras Llunell, Albert, Rodríguez Carbonell, Enric   +3 more
openaire   +2 more sources

Using Problem Frames with Distributed Architectures:

, 2008
Certain classes of problems amenable to description using Problem Frames, in particular ones intended to be implemented using a distributed architecture, can benefit by the addition of a cardinality specification on the domain interfaces.
Cardinality Interfaces
core  

Cardinality of miRNA Datasets.

, 2016
Cardinality of miRNA Datasets.
Alessandra Mezzelani (2170933), Martina Landini (2170930), Federica Viti (31135), Luciano Milanesi (28769), Loredana Petecchia (2170927), Silvia Scaglione (31133)   +5 more
core   +1 more source

Streamlining Diagnosis of Bardet–Biedl Syndrome: New Diagnostic Algorithm With Updated Criteria

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Considerable advances have been made in our understanding of Bardet–Biedl syndrome (BBS), particularly in its core clinical features and molecular genetics, warranting an update to the existing diagnostic criteria framework. Using a rigorous, evidence‐based, and consensus‐driven process, a multidisciplinary group of international experts and ...
Jeremy J. Pomeroy, Jesse Richards, Brooke R. Sweeney, Seema Kumar, Katie E. Queen, Joshua Zaritsky, Carl H. Cramer, Elias I. Traboulsi, Brittni A. Scruggs, Erica E. Davis, Ekaterina Keifer, Emma McGibbon, Timothy Ogden, Bendert De Graaf, Tonia Hymers, Elizabeth Forsythe, Philip Beales   +16 more
wiley   +1 more source

Cardinality of sets associated to b_3 and b_4 sets [PDF]

, 2012
A subset $\mathcal{A}$ of a finite abelian group $(G,+)$ is called a $B_h$ set on $G$ if all sums of $h$ elements of $\mathcal{A}$ are different. In this paper we state closed formulas for the cardinality of some sets associated with $B_3$ and $B_4$ sets,
Ruiz, Diego F., Trujillo, Carlos A., Bravo, Jhon J.   +2 more
core  

Distinct Neuropsychiatric Profiles Associated With 17p11.2 Deletions and RAI1 Variants in Smith–Magenis Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Smith–Magenis syndrome (SMS) results from either a recurrent 17p11.2 deletion or pathogenic variants in the retinoic acid induced 1 gene (RAI1). While neurodevelopmental impairment and behavioral dysregulation are well recognized, systematic genotype‐stratified analyses across psychiatric domains remain limited.
Albin Blanc, Christophe Nemos, Céline Bonnet, Mathilde Renaud, Sandra Chapuis, Pauline Boiroux, Marie‐Noëlle Babinet, Caroline Demily   +7 more
wiley   +1 more source

Reflexivity and Duplicability in Set Theory

Mathematics
Set reflexivity and duplicability are considered by showing, with different proofs, their equivalence with Dedekind’s infinity. Then, an easy derivation of the Schröder–Bernstein theorem is presented, a fundamental result in the theory of cardinal ...
Vincenzo Manca
doaj   +1 more source