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Response to Growth Hormone Treatment in a Patient with Insulin-Like Growth Factor 1 Receptor Deletion

We report a six-year-old boy who presented with short stature, microcephaly, dysmorphic features, and developmental delay and who was identified with a terminal deletion of 15q26.2q26.3 containing the insulin-like growth factor receptor (IGF1R) gene in addition to a terminal duplication of the 4q35....

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Detalles Bibliográficos
Autores principales:	Mahmoud, Ranim, Naidu, Ajanta, Risheg, Hiba, Kimonis, Virginia
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Galenos Publishing 2017
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5785648/ https://www.ncbi.nlm.nih.gov/pubmed/28720553 http://dx.doi.org/10.4274/jcrpe.4456

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