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Design of a prolonged release matrix system based on chitosan of chilean production
(1995)
The objectives of this work were to establish the utility of chitosan of Chilean production, as an excipient suitable for producing a prolonged-release hydrophilic matrix, and to compare two matrix systems, one with chitosan ...
Translocation (11;19)(q23;p13.3) associated with a novel t(5;16) (ql3;q22) in a patient with acute myelocytic leukemia
(Elsevier B.V., 2003-02-01)
A novel association of t(11;19)(q23;p13) and t(5;16)(q13;q22) was detected by G-banding and spectral karyotyping studies in an 18-year-old patient. While balanced t(11; 19) has been often described in acute myelocytic ...
B2B para Q-flow
(UR. FI-INCO,, 2002)
El proyecto "B2B para Q-flow" estudia el problema de integrar un sistema de Workflow con aplicaciones empresariales. El mismo propone desarrollar un módulo para Q-flow, el sistema de Workflow de Urudata, que permita integrar ...
Impacto das variações de número de cópias (CNVs) da região 22q11.2 na população geral e atuação de CNVs modificadoras na síndrome da deleção 22q11.2
(Universidade Federal de São Paulo, 2023-01-24)
A região 22q11.2 é altamente complexa e predisposta à ocorrência de rearranjos genômicos como deleções e duplicações. Essas variantes genéticas, as chamadas variações de número de cópias (CNVs), têm o potencial de acarretar ...
Análise citogenética em alta resolução de 2q37 e 22q13 e molecular do gene SHANK3 em doenças do espectro autístico
(Universidade Estadual Paulista (UNESP), 2014)
22q11 deletion syndrome and limb anomalies: Report on two Brazilian patients
(ALLIANCE COMMUNICATIONS GROUP DIVISION ALLEN PRESS, 2008)
Objective: To report on two Brazilian patients with chromosome 22q11 deletion who presented with velopharyngeal insufficiency, congenital heart anomalies, developmental delay, and limb anomalies. The pattern of limb anomalies ...
Trisomy 1q32 and monosomy 11q25 associated with congenital heart defect: cytogenomic delineation and patient fourteen years follow-up
(2014-08-22)
Abstract
Background
Partial duplication 1q is a rare cytogenetic anomaly frequently associated to deletion of another chromosome, making it difficult to define the precise ...
Cada Q in the eastern Caribbean, West Indies
(Geophysical Journal International (1993) Volume 112, issue #3 pages 507-516, 2010-06-21)
Coda Q, Qc, has been estimated from seismograms of local earthquakes recorded on short-period seismographs on some of the eastern Caribbean islands of the Lesser Antilles arc, West Indies, using the S-S single-scattering ...
Impaired acuity of the approximate number system in 22q11.2 microdeletion syndrome
(2014)
A magnitude comparison deficit has been frequently observed in velocardiofacial syndrome (Del22q11.2). We hypothesized that this deficit extends to impairments in the acuity of the approximate number system (ANS). Three ...
Detección de la microdeleción 22q11.2 por hibridación fluorescente in situ (FISH) en recién nacidos con cardiopatías congénitas aparentemente no sindrómicas
(Biblioteca Digital wdg.biblioUniversidad de Guadalajara, 2021-02-01)