Zobrazeno 1 - 4
of 4
pro vyhledávání: '"María Calvente"'
Autor:
Leandro Landera, Julián Nevado, Juan C. Cigudosa, Sergio Ramos, Jair Tenorio, Irene Dapía, Antonio González-Meneses, María Calvente, Carlos A. Venegas-Vega, Pedro Arias, Pablo Lapunzina, Alicia Hernández, Luis A. Pérez-Jurado
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5afab8cf14817ff834916320fdb9276
https://doi.org/10.1111/cge.13689/v2/response1
https://doi.org/10.1111/cge.13689/v2/response1
Autor:
Francesco Acquadro, Javier Suela, Carolina Martínez-Laperche, Mercedes Trujillo, Juan C. Cigudosa, Rafael Flores, Sara Alvarez, María Calvente, Juliane Menezes, Rocío Salgado
Publikováno v:
Leukemia & Lymphoma. 55:2652-2655
Acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS) represent a group of heterogeneous diseases with a considerable diversity in molecular pathogenesis and clinical outcomes. Recurrent...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1dc3c43e2c74053881657a27345d383
https://doi.org/10.3109/10428194.2014.891024
https://doi.org/10.3109/10428194.2014.891024
Autor:
María Baquero Cano, M. Carmen Carrascosa Romero, María Calvente, Llanos González Castillo, Rosa García Hoyo, Javier Suela
Publikováno v:
American journal of medical genetics. Part A. (4)
A newborn boy with broad forehead, mild microretrognathia, large hands and feet, arachnodactyly and a cortical thumb also had left renal agenesis, dysgenesis of corpus callosum with psychomotor delay. After olignucleotide array comparative genomic hy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9d9dabc07d15df85643b8e64d0325bb
https://pubmed.ncbi.nlm.nih.gov/22407779
https://pubmed.ncbi.nlm.nih.gov/22407779
Autor:
Carlos A. Venegas-Vega, Irene Dapía, Juan C. Cigudosa, Sergio Ramos, María Calvente, Leandro Landera, Pedro Arias, Antonio González-Meneses, Luis A. Pérez-Jurado, Julián Nevado, Alicia Hernández, Jair Tenorio, Pablo Lapunzina
Publikováno v:
Clinical Genetics. 97(3):467-476
The proximal 19p13.3 microdeletion/microduplication (prox19p13.3del/dup) syndrome is a recently described disorder with common clinical features including developmental delay, intellectual disability, speech delay, facial dysmorphic features with ear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b38fe9e89b2931a4f53247a26b4126e