FUSCO, ILEANA

FUSCO, ILEANA  

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A 5.8 Mb interstitial deletion on chromosome Xq21.1 in a boy with intellectual disability, cleft palate, hearing impairment and combined growth hormone deficiency 1-gen-2015 Giordano, Mara; Gertosio, C; Pagani, S; Meazza, C; Fusco, Ileana; Bozzola, E; Bozzola, M.
Frequency of genetic defects in combined pituitary hormone deficiency: a systematic review and analysis of a multicentre Italian cohort 1-gen-2015 DE RIENZO, Francesca; Mellone, Simona; Bellone, Simonetta; Babu, Deepak; Fusco, Ileana; Prodam, Flavia; Petri, Antonella; Muniswamy, Ranjith; De Luca, Filippo; Salerno, Mariacarolina; Momigliano Richardi, Patricia; Bona, Gianni; Giordano, Mara
Novel Mutations in the GH Gene (GH1) Uncover Putative Splicing Regulatory Elements. 1-gen-2014 Babu, Deepak; Mellone, S; Fusco, Ileana; Petri, Antonella; Walker, Ge; Bellone, Simonetta; Prodam, Flavia; Momigliano Richiardi, P; Bona, Gianni; Giordano, Mara
Search for genomic micro-rearrangements through array-CGH in patients with Intellectual Disability and Multiple Pituitary Hormone Deficiency, with standard and custom-design array platforms. 1-gen-2015 Fusco, Ileana
Testing for the cytosine insertion in the VNTR of the MUC1 gene in a cohort of Italian patients with autosomal dominant tubulointerstitial kidney disease 1-gen-2016 Musetti, Claudio; Babu, Deepak; Fusco, Ileana; Mellone, Simona; Zonta, Andrea; Quaglia, Marco; Cantaluppi, Vincenzo; Stratta, Piero; Giordano, Mara
Variations in the High Mobility Group-A2 Gene (HMGA2) Are Associated With Idiopathic Short Stature (ISS) 1-gen-2016 Fusco, Ileana; Babu, Deepak; Mellone, Simona; Barizzone, Nadia; Prodam, Flavia; Fanelli, Antonella; Muniswamy, Ranjit; Petri, Antonella; Bellone, Simonetta; Bona, Gianni; Giordano, Mara