Matches in Nanopublications for { ?s ?p "[Genes causing nonsyndromic autosomal recessive deafness (DFNB12) and deafness associated with retinitis pigmentosa and vestibular dysfunction (USH1D) were previously mapped to overlapping regions of chromosome 10q21-q22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP562139.RAjC3Rt7fpJqtNF04y-Y6nTqr2d2DOBMfzNcRkAtL2JHE130_assertion description "[Genes causing nonsyndromic autosomal recessive deafness (DFNB12) and deafness associated with retinitis pigmentosa and vestibular dysfunction (USH1D) were previously mapped to overlapping regions of chromosome 10q21-q22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP562139.RAjC3Rt7fpJqtNF04y-Y6nTqr2d2DOBMfzNcRkAtL2JHE130_provenance.
- NP936892.RAeddlhatGb2Ic7pUOBhI8zYUMIXaEwKt1k3P9e9byYKg130_assertion description "[Genes causing nonsyndromic autosomal recessive deafness (DFNB12) and deafness associated with retinitis pigmentosa and vestibular dysfunction (USH1D) were previously mapped to overlapping regions of chromosome 10q21-q22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936892.RAeddlhatGb2Ic7pUOBhI8zYUMIXaEwKt1k3P9e9byYKg130_provenance.
- NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_assertion description "[Genes causing nonsyndromic autosomal recessive deafness (DFNB12) and deafness associated with retinitis pigmentosa and vestibular dysfunction (USH1D) were previously mapped to overlapping regions of chromosome 10q21-q22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_provenance.
- NP301123.RAaGTeLDWW8KrVohjbMbpeLlG8NdnBOn6hMJKONribwMY130_assertion description "[Genes causing nonsyndromic autosomal recessive deafness (DFNB12) and deafness associated with retinitis pigmentosa and vestibular dysfunction (USH1D) were previously mapped to overlapping regions of chromosome 10q21-q22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP301123.RAaGTeLDWW8KrVohjbMbpeLlG8NdnBOn6hMJKONribwMY130_provenance.
- NP745530.RAPfJvR03s16LvemMJLTc-ynPHt49NpmORKfRs6n6x85I130_assertion description "[Genes causing nonsyndromic autosomal recessive deafness (DFNB12) and deafness associated with retinitis pigmentosa and vestibular dysfunction (USH1D) were previously mapped to overlapping regions of chromosome 10q21-q22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP745530.RAPfJvR03s16LvemMJLTc-ynPHt49NpmORKfRs6n6x85I130_provenance.