Benjamin T. Levinson

Pediatrics

700 Childrens Dr
Columbus, OH 43205

Last Updated: 09/26/2026

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Found 3 publications

Candidate gene resequencing to identify rare, pedigree-specific variants influencing healthy aging phenotypes in the long life family study.

Candidate gene resequencing to identify rare, pedigree-specific variants influencing healthy aging phenotypes in the long life family study.

Journal: BMC geriatrics

Published: May 07, 2015

Whole-exome capture and sequencing identifies HEATR2 mutation as a cause of primary ciliary dyskinesia.

Whole-exome capture and sequencing identifies HEATR2 mutation as a cause of primary ciliary dyskinesia.

Journal: American journal of human genetics

Published: June 30, 2012

Population-based rare variant detection via pooled exome or custom hybridization capture with or without individual indexing.

Population-based rare variant detection via pooled exome or custom hybridization capture with or without individual indexing.

Journal: BMC genomics

Published: May 29, 2012

Showing 1-3 of 3

Last Updated: 09/26/2026