Matches in Nanopublications for { ?s ?p "[Thus, chordin is a modifier for the craniofacial anomalies of Tbx1 mutations, demonstrating the existence of a second-site modifier for a specific subset of the phenotypes associated with 22q11DS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP272282.RAthxgNOGbPEH7DoKezTI4VuSGmbpo5Pl5GSYpC0C3q4o130_assertion description "[Thus, chordin is a modifier for the craniofacial anomalies of Tbx1 mutations, demonstrating the existence of a second-site modifier for a specific subset of the phenotypes associated with 22q11DS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP272282.RAthxgNOGbPEH7DoKezTI4VuSGmbpo5Pl5GSYpC0C3q4o130_provenance.
- assertion description "[Thus, chordin is a modifier for the craniofacial anomalies of Tbx1 mutations, demonstrating the existence of a second-site modifier for a specific subset of the phenotypes associated with 22q11DS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Thus, chordin is a modifier for the craniofacial anomalies of Tbx1 mutations, demonstrating the existence of a second-site modifier for a specific subset of the phenotypes associated with 22q11DS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP723450.RApd3uLSNBYyphK5fij1mVuMD-uvEwu1dY2wmjbBPJC3s130_assertion description "[Thus, chordin is a modifier for the craniofacial anomalies of Tbx1 mutations, demonstrating the existence of a second-site modifier for a specific subset of the phenotypes associated with 22q11DS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723450.RApd3uLSNBYyphK5fij1mVuMD-uvEwu1dY2wmjbBPJC3s130_provenance.
- NP722935.RAqk94lLeFy330KpkcNpx7htX6Bmh7w2TI--k9PkfYzA4130_assertion description "[Thus, chordin is a modifier for the craniofacial anomalies of Tbx1 mutations, demonstrating the existence of a second-site modifier for a specific subset of the phenotypes associated with 22q11DS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722935.RAqk94lLeFy330KpkcNpx7htX6Bmh7w2TI--k9PkfYzA4130_provenance.
- NP800411.RA70Kw9PxuIc2BJoqPO1mh3dwUvyUKoE4vJ64OK2H09lA130_assertion description "[Thus, chordin is a modifier for the craniofacial anomalies of Tbx1 mutations, demonstrating the existence of a second-site modifier for a specific subset of the phenotypes associated with 22q11DS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP800411.RA70Kw9PxuIc2BJoqPO1mh3dwUvyUKoE4vJ64OK2H09lA130_provenance.
- NP722937.RA7IdFjQMUrWCX6OzvRsWcnHlMaOUYdYZhMHi5j14pU20130_assertion description "[Thus, chordin is a modifier for the craniofacial anomalies of Tbx1 mutations, demonstrating the existence of a second-site modifier for a specific subset of the phenotypes associated with 22q11DS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722937.RA7IdFjQMUrWCX6OzvRsWcnHlMaOUYdYZhMHi5j14pU20130_provenance.