Recurrent somatic mutations are rare in patients with cryptic dyskeratosis congenita
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Title
Recurrent somatic mutations are rare in patients with cryptic dyskeratosis congenita
Authors
Keywords
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Journal
LEUKEMIA
Volume -, Issue -, Pages -
Publisher
Springer Nature
Online
2018-04-04
DOI
10.1038/s41375-018-0125-x
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Note: Only part of the references are listed.- Cancer in the National Cancer Institute inherited bone marrow failure syndrome cohort after fifteen years of follow-up
- (2017) Blanche P. Alter et al. HAEMATOLOGICA
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- (2017) Paula Martínez et al. JOURNAL OF CELL BIOLOGY
- Cancer in the National Cancer Institute inherited bone marrow failure syndrome cohort after fifteen years of follow-up
- (2017) Blanche P. Alter et al. HAEMATOLOGICA
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- (2016) Karla Schmitt et al. DEUTSCHE MEDIZINISCHE WOCHENSCHRIFT
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- (2015) D. P. Steensma et al. BLOOD
- Mutant U2AF1 Expression Alters Hematopoiesis and Pre-mRNA Splicing In Vivo
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- Reconstructing the in vivo dynamics of hematopoietic stem cells from telomere length distributions
- (2015) Benjamin Werner et al. eLife
- Bone marrow failure and the telomeropathies
- (2014) D. M. Townsley et al. BLOOD
- Somatic mutations identify a subgroup of aplastic anemia patients who progress to myelodysplastic syndrome
- (2014) A. G. Kulasekararaj et al. BLOOD
- Age-Related Clonal Hematopoiesis Associated with Adverse Outcomes
- (2014) Siddhartha Jaiswal et al. NEW ENGLAND JOURNAL OF MEDICINE
- Revertant Somatic Mosaicism by Mitotic Recombination in Dyskeratosis Congenita
- (2012) Marjolijn C.J. Jongmans et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Clonal Architecture of Secondary Acute Myeloid Leukemia
- (2012) Matthew J. Walter et al. NEW ENGLAND JOURNAL OF MEDICINE
- Recurrent mutations in the U2AF1 splicing factor in myelodysplastic syndromes
- (2011) Timothy A Graubert et al. NATURE GENETICS
- Clinical Effect of Point Mutations in Myelodysplastic Syndromes
- (2011) Rafael Bejar et al. NEW ENGLAND JOURNAL OF MEDICINE
- Cancer in dyskeratosis congenita
- (2009) B. P. Alter et al. BLOOD
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