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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2005 | 1 |
2006 | 1 |
2008 | 1 |
2017 | 1 |
2018 | 1 |
2024 | 0 |
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Spectrum of sequence variations in the FANCA gene: an International Fanconi Anemia Registry (IFAR) study.
Hum Mutat. 2005 Feb;25(2):142-9. doi: 10.1002/humu.20125.
Hum Mutat. 2005.
PMID: 15643609
Genetic subtyping of Fanconi anemia by comprehensive mutation screening.
Ameziane N, Errami A, Léveillé F, Fontaine C, de Vries Y, van Spaendonk RM, de Winter JP, Pals G, Joenje H.
Ameziane N, et al.
Hum Mutat. 2008 Jan;29(1):159-66. doi: 10.1002/humu.20625.
Hum Mutat. 2008.
PMID: 17924555
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A comprehensive approach to identification of pathogenic FANCA variants in Fanconi anemia patients and their families.
Kimble DC, Lach FP, Gregg SQ, Donovan FX, Flynn EK, Kamat A, Young A, Vemulapalli M, Thomas JW, Mullikin JC, Auerbach AD, Smogorzewska A, Chandrasekharappa SC.
Kimble DC, et al.
Hum Mutat. 2018 Feb;39(2):237-254. doi: 10.1002/humu.23366. Epub 2017 Nov 22.
Hum Mutat. 2018.
PMID: 29098742
Free PMC article.
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Evidence for subcomplexes in the Fanconi anemia pathway.
Medhurst AL, Laghmani el H, Steltenpool J, Ferrer M, Fontaine C, de Groot J, Rooimans MA, Scheper RJ, Meetei AR, Wang W, Joenje H, de Winter JP.
Medhurst AL, et al.
Blood. 2006 Sep 15;108(6):2072-80. doi: 10.1182/blood-2005-11-008151. Epub 2006 May 23.
Blood. 2006.
PMID: 16720839
Free PMC article.
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