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

per Lee, Yee Lin, Wu, Loo Ling
Publicat a J ASEAN Fed Endocr Soc (2019)

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

per Chow, Yock-Ping, Abdul Murad, Nor Azian, Mohd Rani, Zamzureena, Khoo, Jia-Shiun, Chong, Pei-Sin, Wu, Loo-Ling, Jamal, Rahman
Publicat a Orphanet J Rare Dis (2017)

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

per Zainuddin, Ani Amelia, Grover, Sonia Regina, Abdul Ghani, Nur Azurah, Wu, Loo Ling, Rasat, Rahmah, Abdul Manaf, Mohd. Rizal, Shamsuddin, Khadijah, Abdullah Mahdy, Zaleha
Publicat a Health Qual Life Outcomes (2020)

Malaysian Females With Congenital Adrenal Hyperplasia: Surgical Outcomes and Attitudes

per 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
Publicat a Front Pediatr (2019)