Data Policy Finder: an easily integratable tool connecting data librarians with researchers to navigate publication requirements von Dellureficio, Anthony J, Willoughby, Eric, Gibson, Donna S

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Challenges in Communicating a Genetic Diagnosis von Cammarata-Scalisi, Francisco, Willoughby, Colin Eric, Romano, Vito, Callea, Michele

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Clinical and Genetic Aspects of Phelan-McDermid Syndrome: An Interdisciplinary Approach to Management von Cammarata-Scalisi, Francisco, Callea, Michele, Martinelli, Diego, Willoughby, Colin Eric, Tadich, Antonio Cárdenas, Araya Castillo, Maykol, Lacruz-Rengel, María Angelina, Medina, Marco, Grimaldi, Piercesare, Bertini, Enrico, Nevado, Julián

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Membranous aplasia cutis congenita in trisomy 18 von Cammarata-Scalisi, Francisco, Diociaiuti, Andrea, de Guerrero, Blanca, Willoughby, Colin Eric, Callea, Michele

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A c.3037G>A mutation in FBN1 gene causing Marfan syndrome with an atypically severe phenotype von Callea, Michele, Eric Willoughby, Colin, Camarata-Scalisi, Francisco, Giovannoni, Isabella, Vinciguerra, Agatino, Yavuz, Izzet, Di Stazio, Mariateresa, Di Iorio, Enzo, Clarich, Gabriella, Benettoni, Alessandra, Galeotti, Angela, Bellacchio, Emanuele

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Development of a Diagnostic Genetic Test for Simplex and Autosomal Recessive Retinitis Pigmentosa von Clark, Graeme Richard, PhD, Crowe, Paul, BSc, Muszynska, Dorota, MSc, O'Prey, Dominic, BSc, O'Neill, Justin, MPhil, Alexander, Sharon, RGN, Willoughby, Colin Eric, MD, FRCOphth, McKay, Gareth John, PhD, Silvestri, Giuliana, MD, FRCS, Simpson, David Arthur, PhD

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Clinical, etiopathogenic, and therapeutic aspects of KID syndrome von Cammarata‐Scalisi, Francisco, Willoughby, Colin Eric, Cárdenas Tadich, Antonio, Labrador, Nancy, Herrera, Adriana, Callea, Michele

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Multisystemic Manifestations in Rare Diseases: The Experience of Dyskeratosis Congenita von Callea, Michele, Martinelli, Diego, Cammarata-Scalisi, Francisco, Grimaldi, Chiara, Jilani, Houweyda, Grimaldi, Piercesare, Willoughby, Colin Eric, Morabito, Antonino

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COVID‐19 and ectodermal dysplasias. Recommendations are necessary von Callea, Michele, Willoughby, Colin Eric, Perry, Diana, Holzer, Ulrike, Fedele, Giulia, Tadich, Antonio Cárdenas, Cammarata‐Scalisi, Francisco

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Molecular diagnosis for heterogeneous genetic diseases with high-throughput DNA sequencing applied to retinitis pigmentosa von Simpson, David Arthur, Clark, Graeme Richard, Alexander, Sharon, Silvestri, Giuliana, Willoughby, Colin Eric

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Mutacion c.3037GA en el gen FBN1 causa sindrome de Marfan con fenotipo atipico severo von Callea, Michele, Willoughby, Colin Eric, Camarata-Scalisi, Francisco, Giovannoni, Isabella, Vinciguerra, Agatino, Yavuz, Izzet, Di Stazio, Mariateresa, Di Iorio, Enzo, Clarich, Gabriella, Benettoni, Alessandra, Galeotti, Angela, Bellacchio, Emanuele

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COMPOSITION COMPRISING DIACID DERIVATIVES AND THEIR USE IN THE TREATMENT OF COLLAGENIC EYE DISORDERS von WILLOUGHBY, Colin Eric, WILLIAMS, Rachel Lucinda

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COMPOSITION COMPRISING DIACID DERIVATIVES AND THEIR USE IN THE TREATMENT OF COLLAGENIC EYE DISORDERS von WILLOUGHBY, Colin Eric, WILLIAMS, Rachel Lucinda

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A tape motor von WILLOUGHBY ERIC OSBORNE

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Improvements in or relating to electrostatic filter cartridge and filter von ROLLINSON ERIC WILLOUGHBY

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Wide band cavity type aerial von WILLOUGHBY ERIC OSBORNE

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An improved aerial von WILLOUGHBY ERIC OSBORNE

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An improved wide band cavity type aerial von WILLOUGHBY ERIC OSBORNE

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An improved wide band aerial von WILLOUGHBY ERIC OSBORNE

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Coupling arrangement between aerial and transmission line von WILLOUGHBY ERIC OSBORNE

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