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Author/Creator Tejada, María-Isabel

1. 3p14 De Novo Interstitial Microdeletion in a Patient with Intellectual Disability and Autistic Features with Language Impairment: A Comparison with Similar Cases. (14th May 2015)

Authors:
de la Hoz, Ana Belén; Maortua, Hiart; García-Rives, Ainhoa; Martínez-González, María Jesús; Ezquerra, Maitane; Tejada, María-Isabel
Other Names:
Jetten Anton M. Academic Editor.
Journal:
Case reports in genetics
Issue:
Volume 2015(2015)
Page Start:
Record Type:
Journal Article
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2. Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes. Issue 1 (January 2023)

Authors:
Garcia-Pelaez, José; Barbosa-Matos, Rita; Lobo, Silvana; Dias, Alexandre; Garrido, Luzia; Castedo, Sérgio; Sousa, Sónia; Pinheiro, Hugo; Sousa, Liliana; Monteiro, Rita; Maqueda, Joaquin J; Fernandes, Susana; Carneiro, Fátima; Pinto, Nádia; Lemos, Carolina; Pinto, Carla; Teixeira, Manuel R; Aretz,...
Journal:
Lancet oncology
Issue:
Volume 24:Issue 1(2023)
Page Start:
91
Record Type:
Journal Article
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3. Molecular Testing for Fragile X: Analysis of 5062 Tests from 1105 Fragile X Families—Performed in 12 Clinical Laboratories in Spain. (28th May 2014)

Authors:
Tejada, María-Isabel; Glover, Guillermo; Martínez, Francisco; Guitart, Miriam; de Diego-Otero, Yolanda; Fernández-Carvajal, Isabel; Ramos, Feliciano J.; Hernández-Chico, Concepción; Pintado, Elizabet; Rosell, Jordi; Calvo, María-Teresa; Ayuso, Carmen; Ramos-Arroyo, María-Antonia; Maortua, Hiart; ...
Other Names:
Karaca Emin Academic Editor.
Journal:
BioMed research international
Issue:
Volume 2014(2014)
Page Start:
Record Type:
Journal Article
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