Division of Clinical Genetics
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- 2017
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Near-haploid and low hypodiploid acute lymphoblastic leukemia - two distinct subtypes but consistently poor prognosis
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- Contribution to journal › Article
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Pediatric T-cell acute lymphoblastic leukemia
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- Contribution to journal › Scientific review
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Efficacy versus effectiveness of clinical genetic testing criteria for BRCA1 and BRCA2 hereditary mutations in incident breast cancer
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- Contribution to journal › Article
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Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS and neurological symptoms
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- Contribution to journal › Article
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Mark
Frequent low-level mutations of Protein Kinase D2 in angiolipoma
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- Contribution to journal › Article
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Increased proportion of mature NK cells is associated with successful imatinib discontinuation in chronic myeloid leukemia
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- Contribution to journal › Article
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Evaluation of polygenic risk scores for breast and ovarian cancer risk prediction in BRCA1 and BRCA2 mutation carriers
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- Contribution to journal › Article
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Respiratory chain complex III deficiency due to mutated BCS1L : A novel phenotype with encephalomyopathy, partially phenocopied in a Bcs1l mutant mouse model
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- Contribution to journal › Article
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Corticotroph Pituitary Carcinoma in a Patient With Lynch Syndrome (LS) and Pituitary Tumors in a Nationwide LS Cohort
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- Contribution to journal › Article
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Mark
Primary cells in BCR/FGFR1-positive 8p11 myeloproliferative syndrome are sensitive to dovitinib, ponatinib, and dasatinib
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- Contribution to journal › Article