Matches in Nanopublications for { ?s ?p "[A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP7105.RAk8IWM9RLP81e6zsMDUJhi-W-WyBheEUzLYsjC-C-efM130_assertion description "[A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7105.RAk8IWM9RLP81e6zsMDUJhi-W-WyBheEUzLYsjC-C-efM130_provenance.
- NP877547.RAzPhltFNGKcRM5a38NcGHVwVoaSxL7LAN5G9daoKVAt8130_assertion description "[A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP877547.RAzPhltFNGKcRM5a38NcGHVwVoaSxL7LAN5G9daoKVAt8130_provenance.
- NP777664.RAb4h-nXcm2rLc-ycsL2uLuOxw4jA3jl9plykwG2kH8II130_assertion description "[A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP777664.RAb4h-nXcm2rLc-ycsL2uLuOxw4jA3jl9plykwG2kH8II130_provenance.
- assertion description "[A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_assertion description "[A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_provenance.
- NP6393.RAvP_kNGMQ2xAWlXXsO2sUbhwgohpfCS5NuwYLgdI63Ys130_assertion description "[A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6393.RAvP_kNGMQ2xAWlXXsO2sUbhwgohpfCS5NuwYLgdI63Ys130_provenance.