Items where Author is "Musa, Nurul Huda"

Ahmad Rafie, Nur Nabihah and Yubbu, Putri and Aissvarya, Shankar and Pujita, Rajendran and Musa, Nurul Huda and Mohamed Ibrahim, Noor Haliza and Thilakavathy, Karuppiah (2025) Genetic aspects of congenital heart disease in heterotaxy syndromeAspetos genéticos da cardiopatia congénita na síndrome de heterotaxia. Revista Portuguesa de Cardiologia, 44 (10). pp. 633-648. ISSN 0870-2551; eISSN: 2174-2030

Lee, Yee Lin and Ting, Tzer Hwu and Lim, Chong Teik and Thilakavathy, Karuppiah and Musa, Nurul Huda and Ling, King Hwa (2024) Identification of a novel IGSF1 variant in two Malaysian malesiblings with central hypothyroidism and macroorchidism. Journal of Clinical Research in Pediatric Endocrinology. ISSN 1308-5727; eISSN: 1308-5735

Lee, Yee Lin and Ting, Tzer Hwu and Lim, Chong Teik and Thilakavathy, Karuppiah and Musa, Nurul Huda and Ling, King Hwa (2024) Identification of a novel IGSF1 variant in two Malaysian malesiblings with central hypothyroidism and macroorchidism. Journal of Clinical Research in Pediatric Endocrinology. ISSN 1308-5727; eISSN: 1308-5735

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).

Teh, Hui Wen and Lee, Yee Lin and Musa, Nurul Huda and Thilakavathy, Karuppiah (2024) A rare heterozygous SP7 variant c.1019A>c (p.Glu340Ala) in a Malaysian family with Osteogenesis Imperfecta Type XII: a case report. In: 5th International Symposium on Congenital Anomaly and Developmental Biology (ISCADB) 2024, 15-16 Nov. 2024 (pp. 12-13).