Matches in Nanopublications for { ?s ?p "[A founder mutation in BBS2 is responsible for Bardet-Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP285472.RAdm3IEioPV8f1rBqIL9SLWgG_meJcu2FMUAkH3_DxXuY130_assertion description "[A founder mutation in BBS2 is responsible for Bardet-Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP285472.RAdm3IEioPV8f1rBqIL9SLWgG_meJcu2FMUAkH3_DxXuY130_provenance.
- assertion description "[A founder mutation in BBS2 is responsible for Bardet-Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP824807.RAnjzWBqB2fjnc3F2JcfuE7QWYEAb-ESxqeUeV_PGAt9A130_assertion description "[A founder mutation in BBS2 is responsible for Bardet-Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824807.RAnjzWBqB2fjnc3F2JcfuE7QWYEAb-ESxqeUeV_PGAt9A130_provenance.