Zobrazeno 1 - 10
of 65
pro vyhledávání: '"Teresa, Aravena"'
Publikováno v:
Pensamiento Educativo: Revista de Investigación Educacional Latinoamericana, Vol 54, Iss 1, Pp 1-21 (2017)
La oferta y matrícula de programas de magíster ha tenido un crecimiento significativo en los últimos años. Este crecimiento se ha concentrado preferentemente en algunas áreas de conocimiento y en universidades privadas creadas con posterioridad
Externí odkaz:
https://doaj.org/article/c0d81372b42c45f1bdef08621df0e0c9
Autor:
JUAN FRANCISCO CALDERÓN, ALONSO R PUGA, M. LUISA GUZMÁN, CARMEN PAZ ASTETE, MARTA ARRIAZA, MARIANA ARACENA, TERESA ARAVENA, PATRICIA SANZ, GABRIELA M REPETTO
Publikováno v:
Biological Research, Vol 42, Iss 4, Pp 461-468 (2009)
Microdeletion 22q11 in humans causes velocardiofacial and DiGeorge syndromes. Most patients share a common 3Mb deletion, but the clinical manifestations are very heterogeneous. Congenital heart disease is present in 50-80% of patients and is a signif
Externí odkaz:
https://doaj.org/article/1434e2b2f32b43bb996772f9d9dc75ef
Autor:
Joanna Y.L. Tung, Katta M. Girisha, Paul Kruszka, Nicole Fleischer, Engy A. Ashaat, E.V. Badoe, Dalia Farouk Hussen, Neer Shoba Chitrakar, Angélica Moresco, Neveen A. Ashaat, Olufemi Fasanmade, Siddaramappa J. Patil, Mona O. El Ruby, André Mégarbané, Johnathan Watts, Karen Fieggen, Gary T. K. Mok, Dhanya Yesodharan, Milagros M. Dueñas-Roque, Ezana Lulseged, Cedrik Tekendo-Ngongang, Sarah Savage, Saumya Shekhar Jamuar, Vajira H. W. Dissanayake, Nirmala D. Sirisena, Sultana M.H. Faradz, Antonio Richieri-Costa, Kelly L. Jones, Jasmine Chew Yin Goh, Brenda C. Iriele, María Beatriz de Herreros, Brian H.Y. Chung, Godfrey Mutashambara Rwegerera, María Gabriela Obregon, Yonit A. Addissie, Nydia Rena Benita Sihombing, Teresa Aravena, Shubha R. Phadke, Victoria Huckstadt, C. Sampath Paththinige, Meow-Keong Thong, Neerja Gupta, Agustini Utari, Sheela Nampoothiri, Elizabeth Eberechi Oyenusi, Ekanem N. Ekure, Maximilian Muenke, Rupesh Mishra, Oluwarotimi Bolaji Olopade, Annette Uwineza, Vorasuk Shotelersuk, Ambroise Wonkam
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Am J Med Genet A
Universidade de São Paulo (USP)
instacron:USP
Am J Med Genet A
Turner syndrome (TS) is a common multiple congenital anomaly syndrome resulting from complete or partial absence of the second X chromosome. TS presents with short stature, infertility secondary to ovarian dysgenesis, cardiac and renal anomalies, cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf516dfd88789c7ce7186e90a9e30000
Autor:
Marcela Lagos, Andreina Cattani, Reyes L, Alejandro Martinez-Aguayo, Arriaza M, Hernan Garcia, Mariana Aracena, Cecilia Mellado, Vera A, H Rumié, Lacourt P, Teresa Aravena, Helena Poggi, Avalos C, Mericq, Godoy C
Publikováno v:
Hormone Research in Paediatrics. 84:254-257
Background: Deletions in the SHOX gene are the most frequent genetic cause of Leri-Weill syndrome and Langer mesomelic dysplasia, which are also present in idiopathic short stature. Aim: To describe the molecular and clinical findings observed in 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef4e036fc58c16da63d0f790a76b2b8f
https://doi.org/10.1159/000439109
https://doi.org/10.1159/000439109
Publikováno v:
Pensamiento Educativo: Revista de Investigación Educacional Latinoamericana. 54
La oferta y matrícula de programas de magíster ha tenido un crecimiento significativo en los últimos años. Este crecimiento se ha concentrado preferentemente en algunas áreas de conocimiento y en universidades privadas creadas con posterioridad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15d6e63efd52cc1e64db38c17623f64a
https://doi.org/10.7764/pel.54.1.2017.4
https://doi.org/10.7764/pel.54.1.2017.4
Autor:
Rosa A, Pardo Vargas, Mariana, Aracena, Teresa, Aravena, Carolina, Cares, Fanny, Cortés, Víctor, Faundes, Cecilia, Mellado, Cristóbal, Passalacqua, Patricia, Sanz, Silvia, Castillo Taucher
Publikováno v:
Revista chilena de pediatria. 87(5)
The Genetic Branch of the Chilean Society of Paediatrics, given the draft Law governing the decriminalisation of abortion on three grounds, focusing on the second ground, which considers the "embryo or foetus suffering from a congenital structural an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5532027837e46539ae5ad3d696311597
https://pubmed.ncbi.nlm.nih.gov/27234469
https://pubmed.ncbi.nlm.nih.gov/27234469
Publikováno v:
American Journal of Medical Genetics Part A. 155:2552-2555
The Gorlin-Chaudhry-Moss syndrome (GCMS), was describe initially by Gorlin et al. [Gorlin et al. (1960)] in two sisters with craniosynostosis, hypertrichosis, hypoplastic labia majora, dental defects, eye anomalies, patent ductus arteriosus, and norm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f45d522e91ee18b689911a46daf43371
https://doi.org/10.1002/ajmg.a.34204
https://doi.org/10.1002/ajmg.a.34204
Publikováno v:
Revista médica de Chile. 138:1530-1534
Background About 30% of cases of colon cancer (CC) have a family history of CC, and only 5% are hereditary forms. Hereditary forms have an increased risk of CC and other tumors. Aim To report the molecular and genetic study in two families with hered
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa8ec8bef389be2942611c9de65b2f20
https://doi.org/10.4067/s0034-98872010001300009
https://doi.org/10.4067/s0034-98872010001300009
Autor:
Esteban Hurtado, Francisco Ceric, Ricardo Rosas, Marcela Tenorio, María Teresa Aravena, Catalina Mourgues, Carolina Thibaut
Publikováno v:
Consciousness and Cognition. 19:341-351
This study focuses on Implicit learning (IL) in children. One of the main debates in this field concerns the occurrence of IL indicators in experimental settings and its manifestation in different populations. In this research, we are looking for evi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe7058fe2e21ab037d7bd3ea8cd7c417
https://doi.org/10.1016/j.concog.2009.09.006
https://doi.org/10.1016/j.concog.2009.09.006
Autor:
Carmen Astete, Alonso Puga, Marcela Aracena, Juan F. Calderón, Gabriela M. Repetto, Arriaza M, Maria Luisa Guzman, Patricia Sanz, Teresa Aravena
Publikováno v:
CLINICAL GENETICS
Artículos CONICYT
CONICYT Chile
instacron:CONICYT
Artículos CONICYT
CONICYT Chile
instacron:CONICYT
Patients with chromosome 22q11 deletion syndrome exhibit significant phenotypic variability. Epidemiologic data suggest a higher incidence in Hispanics, but limited clinical information is available from Latin-American patients. We describe the clini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d0ab5f8af43b00d5f251fe57d700a61
https://doi.org/10.1111/j.1399-0004.2009.01234.x
https://doi.org/10.1111/j.1399-0004.2009.01234.x