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Year | Number of Results |
---|---|
1997 | 1 |
2006 | 2 |
2013 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 84529
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Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type I.
Haematologica. 2013 Sep;98(9):1383-7. doi: 10.3324/haematol.2013.089490. Epub 2013 May 28.
Haematologica. 2013.
PMID: 23716552
Free PMC article.
Linkage and mutational analysis of the CDAN1 gene reveals genetic heterogeneity in congenital dyserythropoietic anemia type I.
Ahmed MR, Chehal A, Zahed L, Taher A, Haidar J, Shamseddine A, O'Hea AM, Bienz N, Dgany O, Avidan N, Beckmann JS, Tamary H, Higgs D, Vyas P, Wood WG, Wickramasinghe SN.
Ahmed MR, et al.
Blood. 2006 Jun 15;107(12):4968-9. doi: 10.1182/blood-2006-01-0081.
Blood. 2006.
PMID: 16754775
Free article.
No abstract available.
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Evidence of genetic heterogeneity in congenital dyserythropoietic anaemia type I.
Ahmed MR, Zaki M, Sabry MA, Higgs D, Vyas P, Wood W, Wickramasinghe SN.
Ahmed MR, et al.
Br J Haematol. 2006 May;133(4):444-5; author reply 446. doi: 10.1111/j.1365-2141.2006.06089.x.
Br J Haematol. 2006.
PMID: 16643456
Free article.
No abstract available.
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Non-haematological traits associated with congenital dyserythropoietic anaemia type 1: a new entity emerging.
Sabry MA, Zaki M, al Awadi SA, al Saleh Q, Mattar MS.
Sabry MA, et al.
Clin Dysmorphol. 1997 Jul;6(3):205-12. doi: 10.1097/00019605-199707000-00002.
Clin Dysmorphol. 1997.
PMID: 9220189
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