Resultados da busca - Maryam Razzghy Azar

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  1. 1
    Ethnic-specific distribution of mutations in 716 patients with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency

    Ethnic-specific distribution of mutations in 716 patients with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency por Robert C. Wilson, Saroj Nimkarn, M Dumić, Jihad S. Obeid, Maryam Razzghy Azar, Hossein Najmabadi, Fatemeh Saffari, Maria I. New

    Publicado em 2007
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  2. 2
    Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency

    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 em 2017
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