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Author/Creator Alba, Liliana

1. Genetic characterization of a large cohort of Argentine 21‐hydroxylase Deficiency. (3rd May 2020)

Authors:
Fernández, Cecilia S.; Taboas, Melisa; Bruque, Carlos D.; Benavides‐Mori, Belén; Belli, Susana; Stivel, Mirta; Oneto, Adriana; Pasqualini, Titania; Delea, Marisol; Espeche, Lucía D.; Kolomenski, Jorge E.; Alba, Liliana; Buzzalino, Noemí; Dain, Liliana
Journal:
Clinical endocrinology
Issue:
Volume 93:Number 1(2020)
Page Start:
19
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Isolated p.H62L Mutation in the CYP21A2 Gene in a Simple Virilizing 21-Hydroxylase Deficient Patient. (7th July 2013)

Authors:
Taboas, Melisa; Fernández, Cecilia; Belli, Susana; Buzzalino, Noemi; Alba, Liliana; Dain, Liliana
Other Names:
Fenger M. Academic Editor.; Grant S. F. Academic Editor.; Vogt G. Academic Editor.
Journal:
Case reports in genetics
Issue:
Volume 2013(2013)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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