| Bannayan Riley Ruvalcaba syndrome ZA Latiff, RW Atmawidjaja, RJ RajaLope, SAS Omar, SZS Zakaria, ... Annals of the Academy of Medicine, Singapore 39 (7), 578, 2010 | 10 | 2010 |
| Genetic testing for cancer risk: is the community willing to pay for it? AN Aizuddin, AR Ramdzan, SA Syed Omar, Z Mahmud, ZA Latiff, S Amat, ... International journal of environmental research and public health 18 (16), 8752, 2021 | 5 | 2021 |
| Alpha-thalassemia mental retardation syndrome: A case report of two affected siblings ZA Latiff, SAS Omar, D Lau, SW Wong, LC Ong, DA Aziz, SN Akmal Journal of Pediatric Neurology 11 (01), 067-070, 2013 | 3 | 2013 |
| Willingness to pay for cancer genetic testing in a tertiary healthcare centre AN Aizuddin, SR SAS, AR Ramdzan, SO SA, Z Mahmud, A Latiff, SA Shah, ... IIUM Medical Journal Malaysia 20 (3), 2021 | 1 | 2021 |
| Digenic Inheritance of Heterozygous FANCA and BRCA2 mutations in a VACTERL-H patient NAA Murad, CY Ping, ZZM Rani, SN Nasir, S Shuib, DAA Aziz, H Azhari, ... Asian Journal of Medicine and Biomedicine 3 (2), 35-45, 2019 | | 2019 |
| Mutations in KIF27, GNAS and IFT140 genes in a patient with VACTERL association: a case report. RJ Sulaiman, Siti Aishah, Nor Azian Abdul Murad, Yock Ping Chow, Zam Zureena ... Asia-Pacific Journal of Molecular Medicine 8 (2), 2018 | | 2018 |
| Asian Journal of Medicine and Biomedicine, Vol 3: 2. Open Access AA Aziz, H Azhari, SAS Omar, ZA Latiff, AM ia Yang, R Jamal | | |
