Matches in Nanopublications for { ?s ?p "[Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP365.RAQPge2g-dOfarTRoi0JyatYuqD1p7JfeGHfYpXWwrU2w130_assertion description "[Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP365.RAQPge2g-dOfarTRoi0JyatYuqD1p7JfeGHfYpXWwrU2w130_provenance.
- assertion description "[Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP8551.RAH11z6sdPUzibUgJNmTZBCyawSY2CUwEJgEdFZepa750130_assertion description "[Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8551.RAH11z6sdPUzibUgJNmTZBCyawSY2CUwEJgEdFZepa750130_provenance.
- NP539.RA4o71Jjr_G6S5w86PmUQtOCD-Yv3lAM1SByJHoRCNd44130_assertion description "[Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP539.RA4o71Jjr_G6S5w86PmUQtOCD-Yv3lAM1SByJHoRCNd44130_provenance.
- NP5783.RADHvjbSXkNFOet6cfA5KOKnToPrAVvigCWLrylbF-zMs130_assertion description "[Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5783.RADHvjbSXkNFOet6cfA5KOKnToPrAVvigCWLrylbF-zMs130_provenance.
- NP6809.RACSXaH3_54rYvIKnVVCDiUfTGDdTcR3UAU3GYQ4UzHdI130_assertion description "[Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6809.RACSXaH3_54rYvIKnVVCDiUfTGDdTcR3UAU3GYQ4UzHdI130_provenance.
- NP23991.RA3i87SyrKNqelu7WPjej0PLgFwR951DSUwXU3i8O20aY130_assertion description "[Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP23991.RA3i87SyrKNqelu7WPjej0PLgFwR951DSUwXU3i8O20aY130_provenance.