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Emanuela Scarano

Showing results (41-50 of 44) with videos related to

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Frontiers in Endocrinology|May 13, 2024
Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlationSimona F Madeo, Luca Zagaroli, Sara Vandelli, et al.
European Journal of Human Genetics : EJHG|June 1, 2024
Loss-of-function variants in ERF are associated with a Noonan syndrome-like phenotype with or without craniosynostosisMaria Lisa Dentici, Marcello Niceta, Francesca Romana Lepri, et al.
Orphanet Journal of Rare Diseases|June 14, 2012
The empowerment of translational research: lessons from laminopathiesSara Benedetti, Pia Bernasconi, Enrico Bertini, et al.
Orphanet Journal of Rare Diseases|June 17, 2020
Mowat-Wilson syndrome: growth chartsIvan Ivanovski, Olivera Djuric, Serena Broccoli, et al.
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Showing results (41-50 of 44) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 44 results.
Frontiers in Endocrinology|May 13, 2024
Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlationSimona F Madeo, Luca Zagaroli, Sara Vandelli, et al.
European Journal of Human Genetics : EJHG|June 1, 2024
Loss-of-function variants in ERF are associated with a Noonan syndrome-like phenotype with or without craniosynostosisMaria Lisa Dentici, Marcello Niceta, Francesca Romana Lepri, et al.
Orphanet Journal of Rare Diseases|June 14, 2012
The empowerment of translational research: lessons from laminopathiesSara Benedetti, Pia Bernasconi, Enrico Bertini, et al.
Orphanet Journal of Rare Diseases|June 17, 2020
Mowat-Wilson syndrome: growth chartsIvan Ivanovski, Olivera Djuric, Serena Broccoli, et al.
Pageof 5