Bronwyn Dillon

Publications

4

Citations

15

h-index

2

Publishing journals

4

Years of publications

6

Active since

2020

References

148

Institutions

2

1. Exome sequencing identifies existing and novel variants in a South African cohort presenting with anterior segment dysgenesis
   Gene, Volume 943, Pages 149273-149273, Year 2025
2. STAC3 disorder: a common cause of congenital hypotonia in Southern African patients
   European Journal of Human Genetics, Volume 33, Issue 1, Pages 14-23, Year 2024
3. First African case report of hypoparathyroidism, deafness and renal dysplasia (HDR) syndrome due to inverted duplication and deletion of chromosome 10p
   Egyptian Journal of Medical Human Genetics, Volume 25, Issue 1, Year 2024
4. Endocrine profiling in patients with Fanconi anemia, homozygous for a FANCG founder mutation
   Molecular Genetics & Genomic Medicine, Volume 8, Issue 8, Pages e1351-e1351, Year 2020

No publications in the index yet.