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Diamond–Blackfan anemia with mandibulofacial dystostosis is heterogeneous, including the novel DBA genes TSR2 and RPS28 - Gripp - 2014 - American Journal of Medical Genetics Part A - Wiley Online Library
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Diamond-Blackfan anemia caused by chromosome 1p22 deletion encompassing RPL5 | Human Genome Variation
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Amie Rose has undergone 60 blood transfusions at five because of Diamond Blackfan Anaemia | Daily Mail Online
Diamond-Blackfan anemia: genotype-phenotype correlations in Italian patients with RPL5 and RPL11 mutations | Haematologica
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Medicina | Free Full-Text | Unusual Association of Diamond–Blackfan Anemia and Severe Sinus Bradycardia in a Six-Month-Old White Infant: A Case Report and Literature Review
![Congenital anomalies observed in 56 patients with Diamond Blackfan anemia. | Download Scientific Diagram Congenital anomalies observed in 56 patients with Diamond Blackfan anemia. | Download Scientific Diagram](https://www.researchgate.net/publication/229072709/figure/tbl2/AS:202800270188556@1425362760650/Congenital-anomalies-observed-in-56-patients-with-Diamond-Blackfan-anemia.png)
Congenital anomalies observed in 56 patients with Diamond Blackfan anemia. | Download Scientific Diagram
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PDF] Modeling Diamond-Blackfan Anemia in the Mouse: Disease Pathogenesis and Evaluation of Novel Therapies | Semantic Scholar
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