作者：
Francesca,Piceci-Sparascio [1]
;
Lucia,Micale [2]
;
Barbara,Torres [3]
;
Valentina,Guida [4]
;
Federica,Consoli [5]
;
Isabella,Torrente [6]
;
Annamaria,Onori [7]
;
Emanuela,Frustaci [8]
;
Maria Cecilia,D’Asdia [9]
;
Francesco,Petrizzelli [10]
;
Laura,Bernardini ;
Cecilia,Mancini ;
Fiorenza,Soli ;
Dario,Cocciadiferro ;
Daniele,Guadagnolo ;
Gioia,Mastromoro ;
Carolina,Putotto ;
Franco,Fontana ;
Nicola,Brunetti-Pierri ;
Antonio,Novelli ;
Antonio,Pizzuti ;
Bruno,Marino ;
Maria Cristina,Digilio ;
Tommaso,Mazza ;
Bruno,Dallapiccola ;
Victor Luis,Ruiz-Perez ;
Marco,Tartaglia ;
Marco,Castori ;
Alessandro,De Luca
作者单位：
Department of Pediatrics, Obstetrics and Gynecology,“Sapienza” University of Rome
[1]
Genetics and Rare Diseases Research Division,Ospedale Pediatrico Bambino Gesù
[2]
Laboratory of Bioinformatics,Fondazione IRCCS-Casa Sollievo della Sofferenza
[3]
Instituto de Investigaciones Biomédicas ‘Alberto Sols’
[4]
Division of Medical Genetics,Fondazione IRCCS-Casa Sollievo della Sofferenza
[5]
Medical Genetic Unit,Santa Chiara Hospital APSS
[6]
Laboratory of Medical Genetics, Translational Cytogenomics Research Unit,Bambino Gesù Children
[7]
Department of Experimental Medicine,Sapienza University of Rome
[8]
Pediatric Hospital
[9]
Department of Translational Medicine, Section of Pediatrics,Federico II University
[10]
发布时间
2023-09-09
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