Matches in Nanopublications for { ?s ?p "[X-linked lissencephaly with ambiguous genitalia (XLAG) is a recently described genetic disorder caused by mutation in the aristaless-related homeobox (ARX) gene (Xp22.13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP704599.RAfXAQya9ZnG1CkXVIDtri7ERbWXtkGl0AfglBFCXN0VQ130_assertion description "[X-linked lissencephaly with ambiguous genitalia (XLAG) is a recently described genetic disorder caused by mutation in the aristaless-related homeobox (ARX) gene (Xp22.13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP704599.RAfXAQya9ZnG1CkXVIDtri7ERbWXtkGl0AfglBFCXN0VQ130_provenance.
- NP719088.RAi2KgRgQsnZf7xptC6sUUbFX5tjAy-4oRJsqAjQ4g9w4130_assertion description "[X-linked lissencephaly with ambiguous genitalia (XLAG) is a recently described genetic disorder caused by mutation in the aristaless-related homeobox (ARX) gene (Xp22.13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719088.RAi2KgRgQsnZf7xptC6sUUbFX5tjAy-4oRJsqAjQ4g9w4130_provenance.
- NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_assertion description "[X-linked lissencephaly with ambiguous genitalia (XLAG) is a recently described genetic disorder caused by mutation in the aristaless-related homeobox (ARX) gene (Xp22.13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_provenance.
- assertion description "[X-linked lissencephaly with ambiguous genitalia (XLAG) is a recently described genetic disorder caused by mutation in the aristaless-related homeobox (ARX) gene (Xp22.13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP978198.RAkTPbbt2XJ2o2hPgn_EzoGDuhRJ5bUT3DV3jnrOtASck130_assertion description "[X-linked lissencephaly with ambiguous genitalia (XLAG) is a recently described genetic disorder caused by mutation in the aristaless-related homeobox (ARX) gene (Xp22.13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978198.RAkTPbbt2XJ2o2hPgn_EzoGDuhRJ5bUT3DV3jnrOtASck130_provenance.
- NP588633.RA-UYZAOiJnd6OxmPTH7nK0mlsZwdOkrM9cwyY0ViVqPg130_assertion description "[X-linked lissencephaly with ambiguous genitalia (XLAG) is a recently described genetic disorder caused by mutation in the aristaless-related homeobox (ARX) gene (Xp22.13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588633.RA-UYZAOiJnd6OxmPTH7nK0mlsZwdOkrM9cwyY0ViVqPg130_provenance.