Ms Saba Montazaribarforoushi
NHMRC Grant-Funded Researcher A
School of Medicine
College of Health
| Year | Citation |
|---|---|
| 2025 | Tan, N. B., Jolly, L., Nawaz, U., Zhao, S. F., Gyurkovska, V., Silk, M., . . . White, S. M. (2025). UPF1 variants cause syndromic intellectual disability with a transcriptome profile convergent with fragile X syndrome (Award Candidate). Poster session presented at the meeting of Abstracts from the 58th European Society of Human Genetics (ESHG) Conference as published in European Journal of Human Genetics. United Kingdom: Nature Publishing Group. |
| 2023 | Vikkula, M., Babic, M., Brautigan, P., Haan, E., White, M., Piltz, S., . . . Montazaribarforoushi, S. (2023). A new Smad4 mouse model mimicking Myhre Syndrome?. Poster session presented at the meeting of EUROPEAN JOURNAL OF HUMAN GENETICS. AUSTRIA, Vienna: SPRINGERNATURE. |
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