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Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 2
2017
Khattab, Ahmed; Haider, Shozeb; Kumar, Ameet; Dhawan, Samarth; Alam, Dauood; Romero, Raquel; Burns, James; Li, Di; Estatico, Jessica; Rahi, Simran; Fatima, Saleel; Alzahrani, Ali; Hafez, Mona; Musa, Noha; Azar, Maryam Razzghy; Khaloul, Najoua; Gribaa, Moez; Saad, Ali; Ben Charfeddine, Ilhem; Mendonca, Berenice Bilharinho de; Belgorosky, Alicia; Dumic, Katja; Dumic, Miroslav; Aisenberg, Javier; Kandemir, Nurgun; Alikasifoglu, Ayfer; Ozon, Alev; Gonc, Nazli; Cheng, Tina; Kuhnle-Krahl, Ursula; Cappa, Marco; Holterhus, Paul-Martin; Nour, Munier A.; Pacaud, Daniele; Holtzman, Assaf; Li, Sun; Zaidi, Mone; Yuen, Tony und New, Maria I.
(2017):
Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency.
In: Proceedings of the National Academy of Sciences of the United States of America, Bd. 114, Nr. 10, E1933-E1940
1996
Andersson, Stefan; Geissler, Wayne M.; Wu, Ling; Davis, Daphne L.; Grumbach, Melvin M.; New, Maria I.; Schwarz, Hans P.; Blethen, Sandra L.; Mendonca, Berenice B.; Bloise, Walter; Witchel, Selma F.; Cutler Jr., Gordon B.; Griffin, James E.; Wilson, Jean D. und Russell, David D.
(1996):
Molecular genetics and pathophysiology of 17 beta-hydroxysteroid dehydrogenase 3 deficiency.
In: The Journal of Clinical Endocrinology & Metabolism, Bd. 81, Nr. 1: S. 130-136
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