Roles of Type 1 Insulin-Like Growth Factor (IGF) Receptor and IGF-II in Growth Regulation: Evidence From a Patient Carrying Both an 11p Paternal Duplication and 15q Deletion

We report an original association of complex genetic defects in a patient carrying both an 11p paternal duplication, resulting in the double expression of insulin-like growth factor 2 (IGF2), as reported in Beckwith-Wiedemann syndrome, and a 15q terminal deletion, including the type 1 IGF receptor g...

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Detalles Bibliográficos
Autores principales: Giabicani, Eloïse, Chantot-Bastaraud, Sandra, Bonnard, Adeline, Rachid, Myriam, Whalen, Sandra, Netchine, Irène, Brioude, Frédéric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503735/
https://www.ncbi.nlm.nih.gov/pubmed/31114545
http://dx.doi.org/10.3389/fendo.2019.00263

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503735/
https://www.ncbi.nlm.nih.gov/pubmed/31114545
http://dx.doi.org/10.3389/fendo.2019.00263

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