Matches in Nanopublications for { ?s ?p "[Crouzon Syndrome is an autosomal dominant syndromic craniosynostosis characterized by premature closure of cranial sutures, exophthalmos, and midface hypoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP651841.RAQRVNU4YyqgkqtBubnoofUKhHdTbLeLuR-tfhjJk61uY130_assertion description "[Crouzon Syndrome is an autosomal dominant syndromic craniosynostosis characterized by premature closure of cranial sutures, exophthalmos, and midface hypoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651841.RAQRVNU4YyqgkqtBubnoofUKhHdTbLeLuR-tfhjJk61uY130_provenance.
- NP812436.RAYH623by97WnzJWmW6t4uoJoIht5PcF-qlxmbJhdO-6Y130_assertion description "[Crouzon Syndrome is an autosomal dominant syndromic craniosynostosis characterized by premature closure of cranial sutures, exophthalmos, and midface hypoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP812436.RAYH623by97WnzJWmW6t4uoJoIht5PcF-qlxmbJhdO-6Y130_provenance.
- NP303806.RAwnft_3U2yjGUWZHg0RTWA5XY-Eyjgf5sAdTVTiUtgJ4130_assertion description "[Crouzon Syndrome is an autosomal dominant syndromic craniosynostosis characterized by premature closure of cranial sutures, exophthalmos, and midface hypoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP303806.RAwnft_3U2yjGUWZHg0RTWA5XY-Eyjgf5sAdTVTiUtgJ4130_provenance.
- NP197501.RAH-3CYUdzyvXJDQEH-dD33PXaliIxjH94lqZRd5TyTdc130_assertion description "[Crouzon Syndrome is an autosomal dominant syndromic craniosynostosis characterized by premature closure of cranial sutures, exophthalmos, and midface hypoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP197501.RAH-3CYUdzyvXJDQEH-dD33PXaliIxjH94lqZRd5TyTdc130_provenance.
- NP398116.RAMMibN5iVG0NESt7krBBPHQPJlZT__p5sR6A0EQVxOeo130_assertion description "[Crouzon Syndrome is an autosomal dominant syndromic craniosynostosis characterized by premature closure of cranial sutures, exophthalmos, and midface hypoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP398116.RAMMibN5iVG0NESt7krBBPHQPJlZT__p5sR6A0EQVxOeo130_provenance.