Search

Your search keyword '"Morrisson, Valerie"' showing total 7 results

Search Constraints

Start Over You searched for: Author "Morrisson, Valerie" Remove constraint Author: "Morrisson, Valerie"
7 results on '"Morrisson, Valerie"'

Search Results

1. Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations

2. Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

3. Advertising viewability in online branding campaigns

4. Publisher Correction:Whole-genome sequencing of a sporadic primary immunodeficiency cohort (Nature, (2020), 583, 7814, (90-95), 10.1038/s41586-020-2265-1)

5. Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations

6. Whole-genome sequencing of a sporadic primary immunodeficiency cohort

7. Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

Catalog

Books, media, physical & digital resources