A rare case of Wiskott-Aldrich Syndrome with normal platelet size: a case report

por Baharin, Mohd Farid, Dhaliwal, Jasbir Singh, Sarachandran, Smrdhi V. V., Idris, Siti Zaharah, Yeoh, Seoh Leng
Publicado 2016

A Novel De Novo NFKBIA Missense Mutation Associated to Ectodermal Dysplasia with Dysgammaglobulinemia

por Chear, Chai Teng, El Farran, Bader Abdul Kader, Sham, Marina, Ramalingam, Kavetha, Noh, Lokman Mohd, Ismail, Intan Hakimah, Chiow, Mei Yee, Baharin, Mohd Farid, Ripen, Adiratna Mat, Mohamad, Saharuddin Bin
Publicado 2022

A single‐center pilot study in Malaysia on the clinical utility of whole‐exome sequencing for inborn errors of immunity

por Ripen, Adiratna Mat, Chear, Chai Teng, Baharin, Mohd Farid, Nallusamy, Revathy, Chan, Kwai Cheng, Kassim, Asiah, Choo, Chong Ming, Wong, Ke Juin, Fong, Siew Moy, Tan, Kah Kee, Nachiappan, Jeyaseelan P., Teo, Kai Ru, Chiow, Mei Yee, Hishamshah, Munirah, Ghani, Hamidah, Muralitharan, Rikeish R., Mohamad, Saharuddin Bin
Publicado 2021

Clinical features and mutational analysis of X-linked agammaglobulinemia patients in Malaysia

por Chear, Chai Teng, Ismail, Intan Hakimah, Chan, Kwai Cheng, Noh, Lokman Mohd, Kassim, Asiah, Latiff, Amir Hamzah Abdul, Gill, Sandeep Singh, Ramly, Nazatul Haslina, Tan, Kah Kee, Sundaraj, Charlotte, Choo, Chong Ming, Mohamed, Sharifah Adlena Syed, Baharin, Mohd Farid, Zamri, Amelia Suhana, Yahya, Sharifah Nurul Husna Syed, Mohamad, Saharuddin Bin, Ripen, Adiratna Mat
Publicado 2023