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A duplication%25252Fparacentric inversion associated with fa…
A duplication%25252Fparacentric inversion associated with familial X-linked deafness %252528DFN3%252529 suggests the presence of a regulatory element more than 400 kb upstream of the POU3F4 gene
A duplication%25252Fparacentric inversion associated with familial X-linked deafness %252528DFN3%252529 suggests the presence of a regulatory element more than 400 kb upstream of the POU3F4 gene
Article, Chapter
Authors: Kok
Publication: Human Molecular Genetics
ISSN: 0964-6906
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View Full Text Source:Human Molecular Genetics,Human Molecular Genetics,Oxford University Press Journals (UKB 2021-2023) Opens in new Window
Journal:  Human Molecular Genetics Source:Oxford University Press Journals (UKB 2021-2023) Opens in new Window
Collection:  Oxford University Press Journals (UKB 2021-2023)
Coverage:
  • 1996~present; volume:5~present;issue:1~present
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