1. Méndez, Manuel, Moreno-Carralero, María Isabel, Peri, Valeria L, Alonso-Domínguez, Juan Manuel, Morán-Jiménez, María José. 2020. Congenital dyserythropoietic anemia types Ib, II, and III: novel variants in the CDIN1 gene and functional study of a novel variant in the KIF23 gene. In Annals of hematology, 100, 353-364. doi:10.1007/s00277-020-04319-5. https://pubmed.ncbi.nlm.nih.gov/33159567/
2. Sedor, Samantha F, Shao, Sichen. 2024. Mechanism of ASF1 Inhibition by CDAN1. In bioRxiv : the preprint server for biology, , . doi:10.1101/2024.08.08.607204. https://pubmed.ncbi.nlm.nih.gov/39149339/
3. King, Richard, Gallagher, Patrick J, Khoriaty, Rami. 2021. The congenital dyserythropoieitic anemias: genetics and pathophysiology. In Current opinion in hematology, 29, 126-136. doi:10.1097/MOH.0000000000000697. https://pubmed.ncbi.nlm.nih.gov/35441598/
4. Russo, Roberta, Iolascon, Achille, Andolfo, Immacolata, Marra, Roberta, Rosato, Barbara Eleni. 2024. Updates on clinical and laboratory aspects of hereditary dyserythropoietic anemias. In International journal of laboratory hematology, 46, 595-605. doi:10.1111/ijlh.14307. https://pubmed.ncbi.nlm.nih.gov/38747503/
5. Scott, Caroline, Downes, Damien J, Brown, Jill M, Babbs, Christian, Buckle, Veronica J. 2021. Recapitulation of erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I) identifies defects in differentiation and nucleolar abnormalities. In Haematologica, 106, 2960-2970. doi:10.3324/haematol.2020.260158. https://pubmed.ncbi.nlm.nih.gov/33121234/
6. Marra, Roberta, Nostroso, Antonella, Rosato, Barbara Eleni, Andolfo, Immacolata, Russo, Roberta. 2024. Unveiling the genetic landscape of suspected congenital dyserythropoietic anemia type I: A retrospective cohort study of 36 patients. In American journal of hematology, 99, 1511-1522. doi:10.1002/ajh.27350. https://pubmed.ncbi.nlm.nih.gov/38666530/
7. Zhang, Bin, Liu, Michel, Fong, Chin-To, Iqbal, M Anwar. 2021. MEIS2 (15q14) gene deletions in siblings with mild developmental phenotypes and bifid uvula: documentation of mosaicism in an unaffected parent. In Molecular cytogenetics, 14, 58. doi:10.1186/s13039-021-00570-1. https://pubmed.ncbi.nlm.nih.gov/34930369/
8. Gu, Li-Hong, Wu, Ran-Ran, Zheng, Xin-Li, Peng, Min-Sheng, Ma, Cheng. 2023. Genomic insights into local adaptation and phenotypic diversity of Wenchang chickens. In Poultry science, 103, 103376. doi:10.1016/j.psj.2023.103376. https://pubmed.ncbi.nlm.nih.gov/38228059/