Rahman, Fatima

University of Child Health Sciences

1 paper on CoChatORCID 0000-0003-1312-1007

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

Go further with a free account

Verify every reference, keep papers in a library, and ask questions across them.

Sign up - it is free