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Two Novel Mutations of The LHX3 Gene Associated with a Severe Phenotype Involving Endocrine, Nervous and Skeletal Systems | ESPE2019
Laura Guazzarotti; Sara Azzolini; Sheila Ulivi; Antonella Fabretto; Francesca Riello; Carmela Ardisia
http://abstracts.eurospe.org/hrp/0092/hrp0092LB-22
Published: 2019-08-22

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Epidemiology of Diagnoses of Sex Development Disorders Based on the Registry of Rare Diseases, in a Large Area of North-Eastern Italy | ESPE2019
Laura Guazzarotti; Simona Censi; Joaquin Gutierrez; Sara Azzolini
http://abstracts.eurospe.org/hrp/0092/hrp0092P1-418
Published: 2019-08-22

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Two Novel Mutations of The LHX3 Gene Associated with a Severe Phenotype Involving Endocrine, Nervous and Skeletal Systems | ESPE2019
Laura Guazzarotti; Sara Azzolini; Sheila Ulivi; Antonella Fabretto; Francesca Riello; Carmela Ardisia
http://abstracts.eurospe.org/hrp/0092/hrp0092lb-22.html
Published: 2019-08-22

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Epidemiology of Diagnoses of Sex Development Disorders Based on the Registry of Rare Diseases, in a Large Area of North-Eastern Italy | ESPE2019
Laura Guazzarotti; Simona Censi; Joaquin Gutierrez; Sara Azzolini
http://abstracts.eurospe.org/hrp/0092/hrp0092p1-418.html
Published: 2019-08-22

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Genetic Diagnosis of Congenital Growth Hormone Deficiency by Massive Parallel Sequencing Using a Target Gene Panel | ESPE2016
Marilena Nakaguma; Lima Jorge Alexanr Augusto de; Assis Funari Mariana Ferreira de; Antonio Marcondes Lerario; Azevedo Correa Fe
http://abstracts.eurospe.org/hrp/0086/hrp0086rfc14.4.htm
Published: 2016-08-19

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