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Ana Beatriz Alvarez

Showing results (11-20 of 29) with videos related to

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Revista Paulista De Pediatria : Orgao Oficial Da Sociedade De Pediatria De Sao Paulo|January 16, 2020
TRANSLATION, CULTURAL ADAPTATION, AND EVIDENCE OF INSTRUMENT VALIDITY FOR A MORPHOLOGICAL EXAMINATION PERFORMED IN CHILDREN WITH AUTISM SPECTRUM DISORDERThais Arbocese Zanolla, Eduardo Perrone, Rodrigo Ambrosio Fock, et al.
Clinical Dysmorphology|April 5, 2008
Mandibulofacial dysostosis, acral anomalies and frontonasal dysplasia: a new form of acrofacial dysostosisNara Lygia de Macena Sobreira, Maria Tereza S Alves, Ana Beatriz Alvarez Perez, et al.
Sensors (Basel, Switzerland)|August 29, 2024
Exploratory Analysis Using Deep Learning for Water-Body Segmentation of Peru's High-Mountain Remote Sensing ImagesWilliam Isaac Perez-Torres, Diego Armando Uman-Flores, Andres Benjamin Quispe-Quispe, et al.
Molecular Cytogenetics|May 14, 2015
Terminal 18q deletions are stabilized by neotelomeresRoberta Santos Guilherme, Karen E Hermetz, Patrícia Teixeira Varela, et al.
American Journal of Medical Genetics. Part A|October 3, 2020
Overlapping phenotype comprising Kenny-Caffey type 2 and Sanjad-Sakati syndromes: The first case reportThiago Rodrigues Cavole, Eduardo Perrone, Maria de Fatima de Faria Soares, et al.
American Journal of Medical Genetics. Part A|May 13, 2005
Relationship between polymorphisms in genes involved in homocysteine metabolism and maternal risk for Down syndrome in BrazilLuciana Rodrigues Jacy da Silva, Naja Vergani, Luciano de Camargo Galdieri, et al.
Stem Cell Research|June 1, 2021
Generation of two human induced pluripotent stem cell (hiPSC) lines derived from unrelated Marfan Syndrome patientsJuliana Borsoi, Mariana Morato-Marques, Fabiano de Araújo Tofoli, et al.
Revista Paulista De Pediatria : Orgao Oficial Da Sociedade De Pediatria De Sao Paulo|April 12, 2023
A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2Michele Patricia Migliavacca, Rodrigo Ambrosio Fock, Nadia Almeida, et al.
Arquivos Brasileiros De Cardiologia|December 17, 2005
[Serial clinical and echocardiographic evaluation in children with Marfan syndrome]Victor Manuel Oporto Lopez, Ana Beatriz Alvarez Perez, Valdir Ambrósio Moisés, et al.
American Journal of Medical Genetics. Part A|April 21, 2021
Novel MYT1 variants expose the complexity of oculo-auriculo-vertebral spectrum genetic mechanismsMalú Zamariolli, Bruna Burssed, Mariana Moysés-Oliveira, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Revista Paulista De Pediatria : Orgao Oficial Da Sociedade De Pediatria De Sao Paulo|January 16, 2020
TRANSLATION, CULTURAL ADAPTATION, AND EVIDENCE OF INSTRUMENT VALIDITY FOR A MORPHOLOGICAL EXAMINATION PERFORMED IN CHILDREN WITH AUTISM SPECTRUM DISORDERThais Arbocese Zanolla, Eduardo Perrone, Rodrigo Ambrosio Fock, et al.
Clinical Dysmorphology|April 5, 2008
Mandibulofacial dysostosis, acral anomalies and frontonasal dysplasia: a new form of acrofacial dysostosisNara Lygia de Macena Sobreira, Maria Tereza S Alves, Ana Beatriz Alvarez Perez, et al.
Sensors (Basel, Switzerland)|August 29, 2024
Exploratory Analysis Using Deep Learning for Water-Body Segmentation of Peru's High-Mountain Remote Sensing ImagesWilliam Isaac Perez-Torres, Diego Armando Uman-Flores, Andres Benjamin Quispe-Quispe, et al.
Molecular Cytogenetics|May 14, 2015
Terminal 18q deletions are stabilized by neotelomeresRoberta Santos Guilherme, Karen E Hermetz, Patrícia Teixeira Varela, et al.
American Journal of Medical Genetics. Part A|October 3, 2020
Overlapping phenotype comprising Kenny-Caffey type 2 and Sanjad-Sakati syndromes: The first case reportThiago Rodrigues Cavole, Eduardo Perrone, Maria de Fatima de Faria Soares, et al.
American Journal of Medical Genetics. Part A|May 13, 2005
Relationship between polymorphisms in genes involved in homocysteine metabolism and maternal risk for Down syndrome in BrazilLuciana Rodrigues Jacy da Silva, Naja Vergani, Luciano de Camargo Galdieri, et al.
Stem Cell Research|June 1, 2021
Generation of two human induced pluripotent stem cell (hiPSC) lines derived from unrelated Marfan Syndrome patientsJuliana Borsoi, Mariana Morato-Marques, Fabiano de Araújo Tofoli, et al.
Revista Paulista De Pediatria : Orgao Oficial Da Sociedade De Pediatria De Sao Paulo|April 12, 2023
A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2Michele Patricia Migliavacca, Rodrigo Ambrosio Fock, Nadia Almeida, et al.
Arquivos Brasileiros De Cardiologia|December 17, 2005
[Serial clinical and echocardiographic evaluation in children with Marfan syndrome]Victor Manuel Oporto Lopez, Ana Beatriz Alvarez Perez, Valdir Ambrósio Moisés, et al.
American Journal of Medical Genetics. Part A|April 21, 2021
Novel MYT1 variants expose the complexity of oculo-auriculo-vertebral spectrum genetic mechanismsMalú Zamariolli, Bruna Burssed, Mariana Moysés-Oliveira, et al.
Pageof 3