Sort   by:  
 Page size 
UnknownPrognostic significance of the European LeukemiaNet standardized system for reporting cytogenetic and molecular alterations in adults with acute myeloid leukemia.
Not available
S-EPMC3518729 | biostudies-literature
UnknownDelineation of a Human Mendelian Disorder of the DNA Demethylation Machinery: TET3 Deficiency.
Not available
S-EPMC7010978 | biostudies-literature
UnknownNew York Heart Association functional class predicts exercise parameters in the current era.
Not available
S-EPMC2762947 | biostudies-literature
UnknownThe EN-TEx resource of multi-tissue personal epigenomes & variant-impact models.
Not available
S-EPMC10074325 | biostudies-literature
UnknownExpanded encyclopaedias of DNA elements in the human and mouse genomes.
Not available
S-EPMC7410828 | biostudies-literature
UnknownGenome-wide association study identifies multiple risk loci for renal cell carcinoma.
Not available
S-EPMC5472706 | biostudies-literature
UnknownHigh-throughput discovery of novel developmental phenotypes.
Not available
S-EPMC5295821 | biostudies-literature
UnknownHealth-Status Outcomes with Invasive or Conservative Care in Coronary Disease.
Not available
S-EPMC7261489 | biostudies-literature
UnknownHeterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy.
Not available
S-EPMC6556837 | biostudies-literature
UnknownInitial Invasive or Conservative Strategy for Stable Coronary Disease.
Not available
S-EPMC7263833 | biostudies-literature
Sort   by:  
 Page size