Clinical Features of Girls with Turner Syndrome in a Single Centre in Malaysia

por Lee, Yee Lin, Wu, Loo Ling
Publicado 2019

Exome sequencing identifies SLC26A4, GJB2, SCARB2 and DUOX2 mutations in 2 siblings with Pendred syndrome in a Malaysian family

por Chow, Yock-Ping, Abdul Murad, Nor Azian, Mohd Rani, Zamzureena, Khoo, Jia-Shiun, Chong, Pei-Sin, Wu, Loo-Ling, Jamal, Rahman
Publicado 2017

Health-related quality of life of female patients with congenital adrenal hyperplasia in Malaysia

por Zainuddin, Ani Amelia, Grover, Sonia Regina, Abdul Ghani, Nur Azurah, Wu, Loo Ling, Rasat, Rahmah, Abdul Manaf, Mohd. Rizal, Shamsuddin, Khadijah, Abdullah Mahdy, Zaleha
Publicado 2020

Malaysian Females With Congenital Adrenal Hyperplasia: Surgical Outcomes and Attitudes

por Zainuddin, Ani Amelia, Grover, Sonia Regina, Soon, Chong Hong, Nur Azurah, Abdul Ghani, Mahdy, Zaleha Abdullah, Wu, Loo Ling, Rasat, Rahmah, Harun, Fatimah, Chia, Wee Yan, Shamsuddin, Khadijah
Publicado 2019