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Author/Creator Dain, Liliana

3. CYP21A2 mutation update: Comprehensive analysis of databases and published genetic variants. Issue 1 (6th November 2017)

Authors:
Simonetti, Leandro; Bruque, Carlos D.; Fernández, Cecilia S.; Benavides‐Mori, Belén; Delea, Marisol; Kolomenski, Jorge E.; Espeche, Lucía D.; Buzzalino, Noemí D.; Nadra, Alejandro D.; Dain, Liliana
Journal:
Human mutation
Issue:
Volume 39:Issue 1(2018)
Page Start:
5
Record Type:
Journal Article
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4. 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
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Available online (eLD content is only available in our Reading Rooms) ↗

6. 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
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7. Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomalies. (24th January 2018)

Authors:
Portnoi, Marie-France; Dumargne, Marie-Charlotte; Rojo, Sandra; Witchel, Selma F; Duncan, Andrew J; Eozenou, Caroline; Bignon-Topalovic, Joelle; Yatsenko, Svetlana A; Rajkovic, Aleksandar; Reyes-Mugica, Miguel; Almstrup, Kristian; Fusee, Leila; Srivastava, Yogesh; Chantot-Bastaraud, Sandra; Hyon,...
Journal:
Human molecular genetics
Issue:
Volume 27:Number 7(2018:Apr. 01)
Page Start:
1228
Record Type:
Journal Article
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