Evaluating CHARGE syndrome in congenital hypogonadotropic hypogonadism patients harboring CHD7 variants
Xu, Cheng, Cassatella, Daniele, van der Sloot, Almer M, Quinton, Richard, Hauschild, Michael, De Geyter, Christian, Flück, Christa, Feller, Katrin, Bartholdi, Deborah, Nemeth, Attila, Halperin, Irene, Pekic Djurdjevic, Sandra, Maeder, Philippe, Papadakis, Georgios, Dwyer, Andrew A, Marino, Laura, Favre, Lucie, Pignatelli, Duarte, Niederländer, Nicolas J, Acierno, James, Pitteloud, Nelly
Published in Genetics in medicine (01.08.2018)
Published in Genetics in medicine (01.08.2018)
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Developing and evaluating rare disease educational materials co-created by expert clinicians and patients: the paradigm of congenital hypogonadotropic hypogonadism
Badiu, Corin, Bonomi, Marco, Borshchevsky, Ivan, Cools, Martine, Craen, Margarita, Ghervan, Cristina, Hauschild, Michael, Hershkovitz, Eli, Hrabovszky, Erik, Juul, Anders, Kim, Soo-Hyun, Kumanov, Phillip, Lecumberri, Beatriz, Lemos, Manuel C, Neocleous, Vassos, Niedziela, Marek, Djurdjevic, Sandra Pekic, Persani, Luca, Phan-Hug, Franziska, Pignatelli, Duarte, Pitteloud, Nelly, Popovic, Vera, Quinton, Richard, Skordis, Nicos, Smith, Neil, Stefanija, Magdalena Avbelj, Xu, Cheng, Young, Jacques, Dwyer, Andrew A
Published in Orphanet journal of rare diseases (20.03.2017)
Published in Orphanet journal of rare diseases (20.03.2017)
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