Zobrazeno 1 - 10
of 1 005
pro vyhledávání: '"Wilcox ER"'
Autor:
Hotaling S; Department of Watershed Sciences, Utah State University, Logan, UT, USA. scott.hotaling1@gmail.com., Wilcox ER; DNA Sequencing Center, Department of Biology, Brigham Young University, Provo, UT, USA., Heckenhauer J; LOEWE Centre for Translational Biodiversity Genomics (LOEWE-TBG), Frankfurt, Germany.; Department of Terrestrial Zoology, Senckenberg Research Institute and Natural History Museum Frankfurt, 60325, Frankfurt, Germany., Stewart RJ; Department of Biomedical Engineering, University of Utah, Salt Lake City, UT, USA., Frandsen PB; LOEWE Centre for Translational Biodiversity Genomics (LOEWE-TBG), Frankfurt, Germany. paul_frandsen@byu.edu.; Department of Plant and Wildlife Sciences, Brigham Young University, Provo, UT, USA. paul_frandsen@byu.edu.; Data Science Lab, Smithsonian Institution, Washington, DC, USA. paul_frandsen@byu.edu.
Publikováno v:
BMC genomics [BMC Genomics] 2023 Mar 16; Vol. 24 (1), pp. 117. Date of Electronic Publication: 2023 Mar 16.
Autor:
Bhowmik, Oieswarya1 (AUTHOR) oieswarya.bhowmik@wsu.edu, Rahman, Tazin1 (AUTHOR), Kalyanaraman, Ananth1 (AUTHOR)
Publikováno v:
BMC Bioinformatics. 12/4/2024, Vol. 25 Issue 1, p1-27. 27p.
Autor:
Toga, Kouhei1,2 (AUTHOR), Sakamoto, Takuma3 (AUTHOR), Kanda, Miyuki1,4 (AUTHOR), Tamura, Keita1 (AUTHOR), Okuhara, Keisuke2,4 (AUTHOR), Tabunoki, Hiroko3,5 (AUTHOR), Bono, Hidemasa1,2 (AUTHOR) bonohu@hiroshima-u.ac.jp
Publikováno v:
G3: Genes | Genomes | Genetics. Aug2024, Vol. 14 Issue 8, p1-10. 10p.
Autor:
Yousaf R; Laboratory of Molecular Genetics, Department of Otorhinolaryngology - Head and Neck Surgery, University of Maryland, Baltimore, Maryland, USA., Ahmed ZM; Laboratory of Molecular Genetics, Department of Otorhinolaryngology - Head and Neck Surgery, University of Maryland, Baltimore, Maryland, USA., Giese AP; Laboratory of Molecular Genetics, Department of Otorhinolaryngology - Head and Neck Surgery, University of Maryland, Baltimore, Maryland, USA., Morell RJ; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders (NIDCD), NIH, Bethesda, Maryland, USA., Lagziel A; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders (NIDCD), NIH, Bethesda, Maryland, USA., Dabdoub A; Laboratory of Cochlear Development, NIDCD, NIH, Bethesda, Maryland, USA., Wilcox ER; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders (NIDCD), NIH, Bethesda, Maryland, USA., Riazuddin S; Allama Iqbal Medical College, University of Health Sciences, Lahore, Pakistan.; Shaheed Zulfiqar Ali Bhutto Medical University, Pakistan Institute of Medical Sciences, Islamabad, Pakistan., Friedman TB; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders (NIDCD), NIH, Bethesda, Maryland, USA., Riazuddin S; Laboratory of Molecular Genetics, Department of Otorhinolaryngology - Head and Neck Surgery, University of Maryland, Baltimore, Maryland, USA.; Allama Iqbal Medical College, University of Health Sciences, Lahore, Pakistan.; Shaheed Zulfiqar Ali Bhutto Medical University, Pakistan Institute of Medical Sciences, Islamabad, Pakistan.
Publikováno v:
The Journal of clinical investigation [J Clin Invest] 2018 Apr 02; Vol. 128 (4), pp. 1509-1522. Date of Electronic Publication: 2018 Mar 12.
Publikováno v:
Clinical Genetics; Jun2003, Vol. 63 Issue 6, p431-444, 14p
Autor:
Sinninger Y, Attaie A, Walters Fc, M. R. Miller, Mislinski J, Fred H. Linthicum, Anil K. Lalwani, William M. Luxford, Jean K. Moore, Wilcox Er, San Agustin Tb
Publikováno v:
Audiologyneuro-otology. 2(3)
Cochleosaccular dysplasia or degeneration (Scheibe degeneration) is considered the most common cause of profound congenital hearing impairment, and accounts for approximately 70% of cases 2 with hereditary deafness. A five-generation family with here
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::845f791023f93bee3cab202ee1246e90
https://pubmed.ncbi.nlm.nih.gov/9390828
https://pubmed.ncbi.nlm.nih.gov/9390828
Autor:
Li, Yan-Qiong1,2 (AUTHOR), Ma, Heng3 (AUTHOR), Wang, Qin-Yao1 (AUTHOR), Liu, De-Sheng1,4 (AUTHOR), Wang, Wei1 (AUTHOR), Li, Shi-Xin1 (AUTHOR), Zuo, Rong-Xia1 (AUTHOR), Shen, Tao1 (AUTHOR), Zhu, Bao-Sheng5 (AUTHOR), Sa, Ya-Lian1 (AUTHOR) sayalian@126.com
Publikováno v:
BMC Medical Genomics. 2/20/2024, Vol. 17 Issue 1, p1-9. 9p.
Autor:
Zheng, Kaifeng1 (AUTHOR), Lin, Sheng2 (AUTHOR), Gao, Jian1 (AUTHOR), Chen, Shiguo1 (AUTHOR), Su, Jindi1 (AUTHOR), Liu, Zhiqiang2 (AUTHOR), Duan, Shan1 (AUTHOR) shanduan@hotmail.com
Publikováno v:
BMC Medical Genomics. 1/2/2024, Vol. 17 Issue 1, p1-10. 10p.
Publikováno v:
Iranian Journal of Otorhinolaryngology. Jan2024, Vol. 36 Issue 1, p355-360. 6p.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.