Resultados de búsqueda - Abdullah, Wafa
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Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11β-hydroxysteroid dehydrogenase type 2 deficiency por Yau, Mabel, Haider, Shozeb, Khattab, Ahmed, Ling, Chen, Mathew, Mehr, Zaidi, Samir, Bloch, Madison, Patel, Monica, Ewert, Sinead, Abdullah, Wafa, Toygar, Aysenur, Mudryi, Vitalii, Al Badi, Maryam, Alzubdi, Mouch, Wilson, Robert C., Al Azkawi, Hanan Said, Ozdemir, Hatice Nur, Abu-Amer, Wahid, Hertecant, Jozef, Razzaghy-Azar, Maryam, Funder, John W., Al Senani, Aisha, Sun, Li, Kim, Se-Min, Yuen, Tony, Zaidi, Mone, New, Maria I.
Publicado 2017Texto