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Giacomozzi, C., Pedicelli, S., Deodati, A., Pampanini, V., Peschiaroli, E., Spadoni, G.l., et al. (2012). Growth hormone deficiency associated with pituitary abnormalities in 14q microdeletion syndrome: a new phenotype-genotype correlation?. In European Society for Paediatric Endocrinology (ESPE): 51st annual meeting, Leipzig, September 2012: abstracts. Supplement issue: Hormone research in paediatrics, Vol. 78 (2012), Suppl. 1. Karger.

Growth hormone deficiency associated with pituitary abnormalities in 14q microdeletion syndrome: a new phenotype-genotype correlation?

Deodati, A;SPADONI, GIAN LUIGI;SCIRE', GIUSEPPE;CIANFARANI, STEFANO
2012-01-01
Annual meeting of the European Society for paediatric endocrinology (ESPE)
Leipzig (Germany)
2012
51.
Rilevanza internazionale
2012
Settore MED/38 - PEDIATRIA GENERALE E SPECIALISTICA
English
Intervento a convegno
Giacomozzi, C., Pedicelli, S., Deodati, A., Pampanini, V., Peschiaroli, E., Spadoni, G.l., et al. (2012). Growth hormone deficiency associated with pituitary abnormalities in 14q microdeletion syndrome: a new phenotype-genotype correlation?. In European Society for Paediatric Endocrinology (ESPE): 51st annual meeting, Leipzig, September 2012: abstracts. Supplement issue: Hormone research in paediatrics, Vol. 78 (2012), Suppl. 1. Karger.
Giacomozzi, C; Pedicelli, S; Deodati, A; Pampanini, V; Peschiaroli, E; Spadoni, Gl; Scire', G; Cianfarani, S
02 - Intervento a convegno
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/78236
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