Matches in Nanopublications for { ?s ?p "[Through exome sequencing we identified compound heterozygous mutations in WDR19 in a Norwegian family with Sensenbrenner syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP505229.RA8yEetDiGE7nxKLqaD5xu_zdILSQu_ehtU5TkxEEdbSo130_assertion description "[Through exome sequencing we identified compound heterozygous mutations in WDR19 in a Norwegian family with Sensenbrenner syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP505229.RA8yEetDiGE7nxKLqaD5xu_zdILSQu_ehtU5TkxEEdbSo130_provenance.
- NP933093.RAeUMTNB5jA1A9OpkS2K4bm-0_fYwXjILhKEOkA2qUz7I130_assertion description "[Through exome sequencing we identified compound heterozygous mutations in WDR19 in a Norwegian family with Sensenbrenner syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP933093.RAeUMTNB5jA1A9OpkS2K4bm-0_fYwXjILhKEOkA2qUz7I130_provenance.
- assertion description "[Through exome sequencing we identified compound heterozygous mutations in WDR19 in a Norwegian family with Sensenbrenner syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP932809.RAoJ7sQ1FJ641ph1DAJUG5e8x0zg-Dvb7cKaWqxU_rjuk130_assertion description "[Through exome sequencing we identified compound heterozygous mutations in WDR19 in a Norwegian family with Sensenbrenner syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932809.RAoJ7sQ1FJ641ph1DAJUG5e8x0zg-Dvb7cKaWqxU_rjuk130_provenance.