Resultados de búsqueda - Simran Rahi
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Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency por Ahmed Khattab, Shozeb Haider, Ameet Kumar, Samarth Dhawan, Dauood Alam, Raquel Escutia Romero, James Burns, Li Di, Jessica Estatico, Simran Rahi, Saleel Fatima, Ali S. Alzahrani, Mona Hafez, Noha Musa, Maryam Razzghy Azar, Najoua Khaloul, Moez Gribaa, Ali Saâd, Ilhem Ben Charfeddine, Berenice B. Mendonça, Alicia Belgorosky, Katja Dumić, Miroslav Dumić, Javier Aisenberg, Nurgün Kandemir, Ayfer Alikaşifoğlu, Alev Özön, Nazlı Gönç, Tina Cheng, Ursula Kuhnle-Krahl, Marco Cappa, Paul-Martin Holterhus, Munier Nour, Danièle Pacaud, Assaf Holtzman, Li Sun, Mone Zaidi, Tony Yuen, Maria I. New
Publicado 2017Artigo