Bakaeean, Behnaz
Islamic Azad University, Tehran · Islamic Azad University, Science and Research Branch
2 papers on CoChatORCID 0000-0003-0870-4419
Most cited papers
- Verified
Broadening the phenotypic and molecular spectrum of FINCA syndrome: Biallelic NHLRC2 variants in 15 novel individuals
Sczakiel, H. L., Zhao, M., Wollert-Wulf, B., Danyel, M., Ehmke, N., Stoltenburg, C., Damseh, N., Al-Ashhab, M., Balci, T. B., Osmond, M., et al. (2023) · European Journal of Human Genetics
Genomics and Rare DiseasesGenetics and Neurodevelopmental Disorders
Cited by 8
- Verified
FINCA syndrome beyond pulmonary affection: biallelic NHLRC2 variants in eight families with intellectual disability and epilepsy
Boschann, F., Sczakiel, H., Zhao, M., Danyel, M., Stoltenburg, C., Damseh, N., Ashhab, M., Balci, T., Engelen, K. V., Osmond, M., et al. (2022) · European Journal of Human Genetics
Genomics and Rare DiseasesGenetics and Neurodevelopmental Disorders
Cited by 8
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