UPM Institutional Repository

Items where Author is "Shankar, Aissvarya"

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Item Type | No Grouping
Number of items: 2.

Karuppiah, Thilakavathy and Ling, King Hwa and Lim, Chong Teik and Shankar, Aissvarya and Thong, Meow Keong and Abdul Aziz, Noraishah Mydin (2024) Biallelic variants in GLB1 causes GM1-gangliosidosis disease in a family with two siblings. In: 1st International Symposium and Workshop, Medical Genetics Update: From Genomics to Clinic, 16-18 May. 2024, Universitas YARSI, Indonesia. (pp. 98-99). (Submitted)

Karuppiah, Thilakavathy and Mohamed Ibrahim, Noor Haliza and Musa, Nurul Huda and Shankar, Aissvarya and Ahmad Asnawi, Asral Wirda and Yap, Mandy Yee Yee and Sathar, Jameela and Selvaratnam, Veena and Noor Alif Wira, Nurul Ain Suraya (2024) Variant identification using whole exome sequencing in a family suspected with Iron-refractory Iron Deficiency Anaemia. In: 14th Malaysian Symposium of Biomedical Science 2024, 1-2 Jun 2024, Universiti Putra Malaysia, Serdang. (p. 40).

This list was generated on Thu Apr 24 13:26:44 2025 +08.