Sort   by:  
 Page size 
UnknownThe contribution of de novo coding mutations to meningomyelocele.
Not available
S-EPMC12625549 | biostudies-literature
UnknownGenotype, oxidase status, and preceding infection or autoinflammation do not affect allogeneic HCT outcomes for CGD.
Not available
S-EPMC10862239 | biostudies-literature
UnknownIntegrated (epi)-Genomic Analyses Identify Subgroup-Specific Therapeutic Targets in CNS Rhabdoid Tumors.
Not available
S-EPMC5500911 | biostudies-literature
UnknownBi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes.
Not available
S-EPMC6408318 | biostudies-literature
Sort   by:  
 Page size