This VIAF Cluster has been deleted. It is no longer part of VIAF.
Sung, Chun
VIAF ID: 102145003282361301368 ( Unknown Name Type )
Permalink: http://viaf.org/viaf/102145003282361301368
Preferred Forms
- 100 0 _ ‡a Sung Chun
- 100 1 _ ‡a Sung, Chun
4xx's: Alternate Name Forms (2)
Works
Title | Sources |
---|---|
An argument for early genomic sequencing in atypical cases: a WISP3 variant leads to diagnosis of progressive pseudorheumatoid arthropathy of childhood. | |
Genes with monoallelic expression contribute disproportionately to genetic diversity in humans | |
Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans. | |
Genome-wide patterns and properties of de novo mutations in humans. | |
Identification of deleterious mutations within three human genomes. | |
Limited statistical evidence for shared genetic effects of eQTLs and autoimmune-disease-associated loci in three major immune-cell types. | |
Minke whale genome and aquatic adaptation in cetaceans | |
Mitigating false-positive associations in rare disease gene discovery | |
Using whole-genome sequences of the LG/J and SM/J inbred mouse strains to prioritize quantitative trait genes and nucleotides. |