6 results on '"Messiaen, P."'
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2. Single-cell profiling of myeloid cells in glioblastoma across species and disease stage reveals macrophage competition and specialization
3. Constitutional mismatch repair deficiency is the diagnosis in 0.41% of pathogenic NF1/SPRED1 variant negative children suspected of sporadic neurofibromatosis type 1
4. Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation
5. Correction: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation
6. Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas
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