Zobrazeno 1 - 9
of 9
pro vyhledávání: '"A. Pedraza-Meléndez"'
Autor:
A. Martínez-Hernández, D. Martínez-Anaya, C. Durán-McKinster, V. Del Castillo-Ruiz, P. Navarrete-Meneses, E. J. Córdova, B. E. Villegas-Torres, A. Ruiz-Herrera, R. Juárez-Velázquez, E. Yokoyama-Rebollar, D. Cervantes-Barragán, A. Pedraza-Meléndez, L. Orozco, P. Pérez-Vera, C. Salas-Labadía
Publikováno v:
BMC Medical Genomics, Vol 15, Iss 1, Pp 1-11 (2022)
Abstract Background To date, only twenty-one cases diagnosed postnatally with mosaic trisomy 12 have been reported. The most frequent phenotypic manifestations are developmental delay, dysmorphic facial features, congenital heart defects, digital alt
Externí odkaz:
https://doaj.org/article/0c4863867a0d412793d8ded32d6ea797
Autor:
C. Salas-Labadía, S. Gómez-Carmona, R. Cruz-Alcívar, D. Martínez-Anaya, V. Del Castillo-Ruiz, C. Durán-McKinster, V. Ulloa-Avilés, E. Yokoyama-Rebollar, A. Ruiz-Herrera, P. Navarrete-Meneses, E. Lieberman-Hernández, A. González-Del Angel, D. Cervantes-Barragán, C. Villarroel-Cortés, A. Reyes-León, D. Suárez-Pérez, A. Pedraza-Meléndez, A. González-Orsuna, P. Pérez-Vera
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-11 (2019)
Abstract Background Pigmentary mosaicism constitutes a heterogeneous group of skin pigmentation alterations associated with multisystem involvement. The aim of this study was to establish a complete cytogenetic and molecular characterization of PM pa
Externí odkaz:
https://doaj.org/article/3f654e9d49a44d4795a0f54cee82e329
Akademický článek
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Autor:
Roberto Cruz-Alcívar, P. Navarrete-Meneses, A. Reyes-León, A. González-Del Angel, V. Ulloa-Avilés, Patricia Pérez-Vera, A. I. Pedraza-Meléndez, A. González-Orsuna, S. Gómez-Carmona, Consuelo Salas-Labadía, David E. Cervantes-Barragán, Emiy Yokoyama-Rebollar, Esther Lieberman-Hernández, Adriana Ruiz-Herrera, Carola Durán-McKinster, D. Martínez-Anaya, V. Del Castillo-Ruiz, D. Suárez-Pérez, C. Villarroel-Cortés
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-11 (2019)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Pigmentary mosaicism constitutes a heterogeneous group of skin pigmentation alterations associated with multisystem involvement. The aim of this study was to establish a complete cytogenetic and molecular characterization of PM patients, e
Autor:
C. Salas-Labadía, A. I. Pedraza-Meléndez, P. Pérez-Vera, María del Pilar Navarrete-Meneses, D. Moreno-Lorenzana
Publikováno v:
Journal of Applied Toxicology. 38:1262-1270
Pesticides are commonly used worldwide and almost every human is potentially exposed to these chemicals. Exposure to pesticides such as permethrin and malathion has been associated with hematological malignancies in epidemiological studies. However,
Autor:
C. Salas-Labadía, S. Gómez-Carmona, R. Cruz-Alcívar, D. Martínez-Anaya, V. Castillo-Ruiz, C. Durán-McKinster, V. Ulloa-Avilés, E. Yokoyama-Rebollar, A. Ruiz-Herrera, P. Navarrete-Meneses, E. Lieberman-Hernández, A. González-Del Angel, D. Cervantes-Barragán, C. Villarroel-Cortés, A. Reyes-León, D. Suárez-Pérez, A. Pedraza-Meléndez, A. González-Orsuna, P. Pérez-Vera
Additional file 1. “Cytogenetic alterations and molecular analysis detailed description”. The detailed descriptions of the abnormal karyotypes and molecular analysis in association with phenotype in 24 patients with chromosomal abnormalities.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aae7b9ec22fdca2e539f81b055c4fc05
Autor:
M P, Navarrete-Meneses, A I, Pedraza-Meléndez, C, Salas-Labadía, D, Moreno-Lorenzana, P, Pérez-Vera
Publikováno v:
Journal of applied toxicology : JAT. 38(9)
Pesticides are commonly used worldwide and almost every human is potentially exposed to these chemicals. Exposure to pesticides such as permethrin and malathion has been associated with hematological malignancies in epidemiological studies. However,
Akademický článek
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Akademický článek
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