Resultats de la cerca - Abdullah, Wafa
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Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11β-hydroxysteroid dehydrogenase type 2 deficiency per 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.
Publicat 2017Text