Search Results - Musa, Nurul Huda
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A rare heterozygous SP7 variant c.1019A>c (p.Glu340Ala) in a Malaysian family with Osteogenesis Imperfecta Type XII: a case report by Teh, Hui Wen, Lee, Yee Lin, Musa, Nurul Huda, Thilakavathy, Karuppiah
Published 2024Get full text
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Genetic aspects of congenital heart disease in heterotaxy syndromeAspetos genéticos da cardiopatia congénita na síndrome de heterotaxia by Ahmad Rafie, Nur Nabihah, Yubbu, Putri, Aissvarya, Shankar, Pujita, Rajendran, Musa, Nurul Huda, Mohamed Ibrahim, Noor Haliza, Thilakavathy, Karuppiah
Published 2025Get full text
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Variant identification using whole exome sequencing in a family suspected with Iron-refractory Iron Deficiency Anaemia by Karuppiah, Thilakavathy, Mohamed Ibrahim, Noor Haliza, Musa, Nurul Huda, Shankar, Aissvarya, Ahmad Asnawi, Asral Wirda, Yap, Mandy Yee Yee, Sathar, Jameela, Selvaratnam, Veena, Noor Alif Wira, Nurul Ain Suraya
Published 2024Get full text
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