Harvard Catalyst Profiles

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Kevin T Booth, Ph.D.

Concepts

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This page shows the publications Kevin Booth has written about Infant, Newborn.
Kevin Booth
Connection Strength
0.059
Infant, Newborn
  1. Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37. Genet Med. 2019 04; 21(4):948-954.
    View in: PubMed
    Score: 0.046
  2. A comparative analysis of genetic hearing loss phenotypes in European/American and Japanese populations. Hum Genet. 2020 Oct; 139(10):1315-1323.
    View in: PubMed
    Score: 0.013
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© 2022 President and Fellows of Harvard College
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.