Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Syndrome and DKC1[original query] |
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Sequence analysis of the shelterin telomere protection complex genes in dyskeratosis congenita. Journal of medical genetics 2011 1 48 (4): 285-8. Savage Sharon A, Giri Neelam, Jessop Lea, Pike Kristen, Plona Teri, Burdett Laurie, Alter Blanche |
DKC1 gene mutations in human sporadic cancer. Histology and histopathology 2013 Mar 28 (3): 3. Penzo M, Casoli L, Ceccarelli C, Treré D, Ludovini V, Crinò L, Montanaro L |
Genomic analysis of bone marrow failure and myelodysplastic syndromes reveals phenotypic and diagnostic complexity. Haematologica 2015 Jan 100 (1): 42-8. Zhang Michael Y, Keel Siobán B, Walsh Tom, Lee Ming K, Gulsuner Suleyman, Watts Amanda C, Pritchard Colin C, Salipante Stephen J, Jeng Michael R, Hofmann Inga, Williams David A, Fleming Mark D, Abkowitz Janis L, King Mary-Claire, Shimamura Aki |
Cancer spectrum and outcomes in the Mendelian short telomere syndromes. Blood 2020 2 135 (22): 1946-1956. Schratz Kristen E, Haley Lisa, Danoff Sonye K, Blackford Amanda L, DeZern Amy E, Gocke Christopher D, Duffield Amy S, Armanios Ma |
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- Page last updated:Apr 16, 2024
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