174 related articles for article (PubMed ID: 9545404)
1. Localization of the gene for congenital dyserythropoietic anemia type I to a <1-cM interval on chromosome 15q15.1-15.3.
Tamary H; Shalmon L; Shalev H; Halil A; Dobrushin D; Ashkenazi N; Zoldan M; Resnitzky P; Korostishevsky M; Bonne-Tamir B; Zaizov R
Am J Hum Genet; 1998 May; 62(5):1062-9. PubMed ID: 9545404
[TBL] [Abstract][Full Text] [Related]
2. Localization of the congenital dyserythropoietic anemia II locus to chromosome 20q11.2 by genomewide search.
Gasparini P; Miraglia del Giudice E; Delaunay J; Totaro A; Granatiero M; Melchionda S; Zelante L; Iolascon A
Am J Hum Genet; 1997 Nov; 61(5):1112-6. PubMed ID: 9345103
[TBL] [Abstract][Full Text] [Related]
3. Localization of the gene for congenital dyserythropoietic anemia type III, CDAN3, to chromosome 15q21-q25.
Lind L; Sandström H; Wahlin A; Eriksson M; Nilsson-Sojka B; Sikström C; Holmgren G
Hum Mol Genet; 1995 Jan; 4(1):109-12. PubMed ID: 7711721
[TBL] [Abstract][Full Text] [Related]
4. Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1.
Dgany O; Avidan N; Delaunay J; Krasnov T; Shalmon L; Shalev H; Eidelitz-Markus T; Kapelushnik J; Cattan D; Pariente A; Tulliez M; Crétien A; Schischmanoff PO; Iolascon A; Fibach E; Koren A; Rössler J; Le Merrer M; Yaniv I; Zaizov R; Ben-Asher E; Olender T; Lancet D; Beckmann JS; Tamary H
Am J Hum Genet; 2002 Dec; 71(6):1467-74. PubMed ID: 12434312
[TBL] [Abstract][Full Text] [Related]
5. [Diagnosis and genetics of congenital dyserythropoietic anemias (CDA)].
Rössler J; Havers W
Klin Padiatr; 2000; 212(4):153-8. PubMed ID: 10994542
[TBL] [Abstract][Full Text] [Related]
6. E109K is a SEC23B founder mutation among Israeli Moroccan Jewish patients with congenital dyserythropoietic anemia type II.
Amir A; Dgany O; Krasnov T; Resnitzky P; Mor-Cohen R; Bennett M; Berrebi A; Tamary H
Acta Haematol; 2011; 125(4):202-7. PubMed ID: 21252497
[TBL] [Abstract][Full Text] [Related]
7. Congenital dyserythropoietic anemias: epidemiology, clinical significance, and progress in understanding their pathogenesis.
Heimpel H
Ann Hematol; 2004 Oct; 83(10):613-21. PubMed ID: 15278299
[TBL] [Abstract][Full Text] [Related]
8. Geographic distribution of CDA-II: did a founder effect operate in Southern Italy?
Iolascon A; Servedio V; Carbone R; Totaro A; Carella M; Perrotta S; Wickramasinghe SN; Delaunay J; Heimpel H; Gasparini P
Haematologica; 2000 May; 85(5):470-4. PubMed ID: 10800161
[TBL] [Abstract][Full Text] [Related]
9. Congenital dyserythropoietic anemia type II: exclusion of seven candidate genes.
Lanzara C; Ficarella R; Totaro A; Chen X; Roberto R; Perrotta S; Lasalandra C; Gasparini P; Iolascon A; Carella M
Blood Cells Mol Dis; 2003; 30(1):22-9. PubMed ID: 12667984
[TBL] [Abstract][Full Text] [Related]
10. Recapitulation of erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I) identifies defects in differentiation and nucleolar abnormalities.
Scott C; Downes DJ; Brown JM; Beagrie R; Olijnik AA; Gosden M; Schwessinger R; Fisher CA; Rose A; Ferguson DJP; Johnson E; Hill QA; Okoli S; Renella R; Ryan K; Brand M; Hughes J; Roy NBA; Higgs DR; Babbs C; Buckle VJ
Haematologica; 2021 Nov; 106(11):2960-2970. PubMed ID: 33121234
[TBL] [Abstract][Full Text] [Related]
11. [Localized gene of the rare "Norrland disease". CDA-III blood disease with dominant heredity].
Sandström H; Wahlin A
Lakartidningen; 1999 Jan; 96(4):343-7. PubMed ID: 10024825
[TBL] [Abstract][Full Text] [Related]
12. Congenital dyserythropoietic anemia type I: report of a pair of siblings in Japan.
Kuribayashi T; Uchida S; Kuroume T; Umegae S; Omine M; Maekawa T
Blut; 1979 Sep; 39(3):201-9. PubMed ID: 476312
[TBL] [Abstract][Full Text] [Related]
13. Exclusion of three candidate genes as determinants of congenital dyserythropoietic anemia type II (CDA-II).
Iolascon A; Miraglia del Giudice E; Perrotta S; Granatiero M; Zelante L; Gasparini P
Blood; 1997 Nov; 90(10):4197-200. PubMed ID: 9354691
[TBL] [Abstract][Full Text] [Related]
14. Angioid streaks are part of a familial syndrome of dyserythropoietic anaemia (CDA III).
Sandström H; Wahlin A; Eriksson M; Holmgren G; Lind L; Sandgren O
Br J Haematol; 1997 Sep; 98(4):845-9. PubMed ID: 9326176
[TBL] [Abstract][Full Text] [Related]
15. The congenital dyserythropoietic anaemias.
Delaunay J; Iolascon A
Baillieres Best Pract Res Clin Haematol; 1999 Dec; 12(4):691-705. PubMed ID: 10895259
[TBL] [Abstract][Full Text] [Related]
16. Congenital dyserythropoietic anemia type 1 with a novel mutation in the CDAN1 gene previously diagnosed as congenital hemolytic anemia.
Fujino H; Doisaki S; Park YD; Hama A; Muramatsu H; Kojima S; Sumimoto S
Int J Hematol; 2013 May; 97(5):650-3. PubMed ID: 23605369
[TBL] [Abstract][Full Text] [Related]
17. Preferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1-cM 15q15.1-q15.3 interval.
Allamand V; Broux O; Richard I; Fougerousse F; Chiannilkulchai N; Bourg N; Brenguier L; Devaud C; Pasturaud P; Pereira de Souza A
Am J Hum Genet; 1995 Jun; 56(6):1417-30. PubMed ID: 7762565
[TBL] [Abstract][Full Text] [Related]
18. Congenital dyserythropoietic anemia type II (CDAII/HEMPAS): where are we now?
Denecke J; Marquardt T
Biochim Biophys Acta; 2009 Sep; 1792(9):915-20. PubMed ID: 19150496
[TBL] [Abstract][Full Text] [Related]
19. Distal limb anomalies in patients with congenital dyserythropoietic anemia.
Amir AZ; Horev G; Yacobovich J; Bennett M; Tamary H
Am J Med Genet A; 2017 Feb; 173(2):487-490. PubMed ID: 27759939
[TBL] [Abstract][Full Text] [Related]
20. Congenital dyserythropoietic anemia in China: a case report from two families and a review.
Ru Y; Liu G; Bai J; Dong S; Nie N; Zhang H; Zhao S; Zheng Y; Zhu X; Nie G; Zhang F; Eyden B
Ann Hematol; 2014 May; 93(5):773-7. PubMed ID: 24196372
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
