HuGE Literature Finder
Records 1-4
Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes.
BMC medical genomics 2018 Sep 11 (1): 77. Lewis Morag A, Nolan Lisa S, Cadge Barbara A, Matthews Lois J, Schulte Bradley A, Dubno Judy R, Steel Karen P, Dawson Sally |
Identification of somatic mutations using whole-exome sequencing in Korean patients with acute myeloid leukemia.
BMC medical genetics 2017 03 18 (1): 23. Heo Seong Gu, Koh Youngil, Kim Jong Kwang, Jung Jongsun, Kim Hyung-Lae, Yoon Sung-Soo, Park Ji W |
Neuronal structural protein polymorphism and concussion in college athletes.
Brain injury 2011 25 (11): 1108-13. McDevitt Jane K, Tierney Ryan T, Mansell Jamie L, Driban Jeffrey B, Higgins Michael, Toone Nieka, Mishra Anarug, Krynetskiy Evge |
Analysis of heavy neurofilament subunit gene polymorphism in Russian patients with sporadic motor neuron disease (MND).
European journal of human genetics : EJHG 2004 Mar 12 (3): 241-4. Skvortsova Veronika, Shadrina Marya, Slominsky Petr, Levitsky Gleb, Kondratieva Ekaterina, Zherebtsova Anna, Levitskaya Nina, Alekhin Alexander, Serdyuk Anna, Limborska Svetla |
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- Page last updated:Jan 15, 2021
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