Matches in Nanopublications for { ?s ?p "[We have identified a homozygous missense mutation in the RAD51C gene in a consanguineous family with multiple severe congenital abnormalities characteristic of FA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP715299.RAw3YquG2cpXUXLUxmzzmCOmdXL5sU2eZqZWBAIT8qNhk130_assertion description "[We have identified a homozygous missense mutation in the RAD51C gene in a consanguineous family with multiple severe congenital abnormalities characteristic of FA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715299.RAw3YquG2cpXUXLUxmzzmCOmdXL5sU2eZqZWBAIT8qNhk130_provenance.
- NP735530.RA_r8YMqY25LufnAdZ37Y30ICOZMaEu1x3dxLC1bELB2g130_assertion description "[We have identified a homozygous missense mutation in the RAD51C gene in a consanguineous family with multiple severe congenital abnormalities characteristic of FA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP735530.RA_r8YMqY25LufnAdZ37Y30ICOZMaEu1x3dxLC1bELB2g130_provenance.
- NP765078.RAzLoY-5d9bz7rSfc4dKiX5xPIh3P8l2po96AQJQ9sP2I130_assertion description "[We have identified a homozygous missense mutation in the RAD51C gene in a consanguineous family with multiple severe congenital abnormalities characteristic of FA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP765078.RAzLoY-5d9bz7rSfc4dKiX5xPIh3P8l2po96AQJQ9sP2I130_provenance.
- assertion description "[We have identified a homozygous missense mutation in the RAD51C gene in a consanguineous family with multiple severe congenital abnormalities characteristic of FA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP663814.RAoR0Yfgaylv_lYlR0z7r7HfnKxfHdYZRiRI-d_te6K3o130_assertion description "[We have identified a homozygous missense mutation in the RAD51C gene in a consanguineous family with multiple severe congenital abnormalities characteristic of FA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP663814.RAoR0Yfgaylv_lYlR0z7r7HfnKxfHdYZRiRI-d_te6K3o130_provenance.
- NP806790.RAr-TMxgRS4hO89G7n53xdV83Co8-fiTbhuDStyqtaWL8130_assertion description "[We have identified a homozygous missense mutation in the RAD51C gene in a consanguineous family with multiple severe congenital abnormalities characteristic of FA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP806790.RAr-TMxgRS4hO89G7n53xdV83Co8-fiTbhuDStyqtaWL8130_provenance.