Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome : refining the ACMG criteria
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Savige, Judy (The University of Melbourne)
;
Storey, Helen (Guy's and St Thomas' NHS Foundation Trust (Regne Unit)) ;
Watson, Elizabeth (South West Genomic Laboratory Hub, North Bristol Trust) ;
Hertz, Jens Michael (Odense University Hospital (Dinamarca)) ;
Deltas, Constantinos (University of Cyprus. Center of Excellence in Biobanking and Biomedical Research and Molecule Medicine Center) ;
Renieri, Alessandra (University of Siena. Medical Genetics) ;
Mari, Francesca (Institute de Pathologie et de Genetique ASBL (Bèlgica). Departement de Biologie Moleculaire) ;
Hilbert, Pascale (Institute de Pathologie et de Genetique ASBL (Bèlgica). Departement de Biologie Moleculaire) ;
Plevova, Pavlina (University Hospital of Ostrava. Department of Medical Genetics, and Department of Biomedical Sciences) ;
Byers, Peter (University of Washington. Departments of Pathology and Medicine) ;
Cerkauskaite, Agne (Vilnius University. Institute of Biomedical Sciences) ;
Gregory, Martin (University of Utah Health. Division of Nephrology) ;
Cerkauskiene, Rimante (Vilnius University. Clinic of Pediatrics) ;
Ljubanović, Danica Galešić (University of Zagreb) ;
Becherucci, Francesca (Nephrology Unit and Meyer Children's University Hospital) ;
Errichiello, Carmela (Nephrology Unit and Meyer Children's University Hospital) ;
Massella, Laura (Bambino Gesù Children's Hospital) ;
Aiello, Valeria (University of Bologna) ;
Lennon, Rachel (The University of Manchester) ;
Hopkinson, Louise (The University of Manchester Sciences, Faculty of Biology Medicine and Health) ;
Koziell, Ania (King's College London) ;
Lungu, Adrian (Fundeni Clinical Institute) ;
Rothe, Hansjorg Martin (Centre for Nephrology and Metabolic Disorders, Weisswasser, Germany) ;
Hoefele, Julia (Technische Universität München. Institut für Humangenetik) ;
Zacchia, Miriam (Nephrology Unit, University of Campania) ;
Martic, Tamara Nikuseva (School of Medicine University of Zagreb) ;
Gupta, Asheeta (Birmingham Children's Hospital) ;
van Eerde, Albertien (Utrecht University. Departments of Genetics and Center for Molecular MedicinE) ;
Gear, Susie (Alport UK) ;
Landini, Samuela (University of Florence. Medical Genetics Unit) ;
Palazzo, Viviana (Meyer Children's University Hospital) ;
al-Rabadi, Laith (University of UTAH. Health Sciences Centre) ;
Claes, Kathleen (University Hospitals Leuven (Bèlgica)) ;
Corveleyn, Anniek (University Hospitals Leuven (Bèlgica)) ;
Van Hoof, Evelien (University Hospitals Leuven (Bèlgica)) ;
van Geel, Micheel (Maastricht University Medical Center) ;
Williams, Maggie (Southmead Hospital) ;
Ashton, Emma (Great Ormond Street Hospital for Children (Londres)) ;
Belge, Hendica (Radboud University Medical Center) ;
Ars, Elisabet (Institut d'Investigació Biomèdica Sant Pau) ;
Bierzynska, Agnieszka (University of Bristol. Bristol Renal Unit, Bristol Medical School) ;
Gangemi, Concetta (University Hospital of Verona (Itàlia)) ;
Lipska-Ziętkiewicz, Beata S. (Medical University of Gdansk. Centre for Rare Diseases, and Clinical Genetics Unit) ;
Universitat Autònoma de Barcelona
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