Hasil Pencarian - Angela D'Eustacchio
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1
Linkage study and exome sequencing identify a BDP1 mutation associated with hereditary hearing loss. oleh Giorgia Girotto, Khalid Abdulhadi, Annalisa Buniello, Diego Vozzi, Danilo Licastro, Angela d'Eustacchio, Dragana Vuckovic, Moza Khalifa Alkowari, Karen P Steel, Ramin Badii, Paolo Gasparini
Diterbitkan 2013-01-01Dapatkan teks lengkap
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2
Dominant inheritance of a novel integrin β3 mutation associated with a hereditary macrothrombocytopenia and platelet dysfunction in two Italian families oleh Paolo Gresele, Emanuela Falcinelli, Silvia Giannini, Pio D’Adamo, Angela D’Eustacchio, Teresa Corazzi, Anna Maria Mezzasoma, Filomena Di Bari, Giuseppe Guglielmini, Luca Cecchetti, Patrizia Noris, Carlo L. Balduini, Anna Savoia
Diterbitkan 2009-05-01Dapatkan teks lengkap
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3
Association analysis of bitter receptor genes in five isolated populations identifies a significant correlation between TAS2R43 variants and coffee liking. oleh Nicola Pirastu, Maarten Kooyman, Michela Traglia, Antonietta Robino, Sara M Willems, Giorgio Pistis, Pio d'Adamo, Najaf Amin, Angela d'Eustacchio, Luciano Navarini, Cinzia Sala, Lennart C Karssen, Cornelia van Duijn, Daniela Toniolo, Paolo Gasparini
Diterbitkan 2014-01-01Dapatkan teks lengkap
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4
Molecular diagnosis of Usher syndrome: application of two different next generation sequencing-based procedures. oleh Danilo Licastro, Margherita Mutarelli, Ivana Peluso, Kornelia Neveling, Nienke Wieskamp, Rossella Rispoli, Diego Vozzi, Emmanouil Athanasakis, Angela D'Eustacchio, Mariateresa Pizzo, Francesca D'Amico, Carmela Ziviello, Francesca Simonelli, Antonella Fabretto, Hans Scheffer, Paolo Gasparini, Sandro Banfi, Vincenzo Nigro
Diterbitkan 2012-01-01Dapatkan teks lengkap
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