Matches in Nanopublications for { ?s ?p "[Three rare autosomal recessive disorders share the combination of congenital muscular dystrophy and brain malformations including a neuronal migration defect: muscle-eye-brain disease (MEB), Walker-Warburg syndrome (WWS), and Fukuyama congenital muscular dystrophy (FCMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP473696.RAAasbQuhcK_PcD3w6zhFs6SrtjIn-mrAvpRgTkBOUBXY130_assertion description "[Three rare autosomal recessive disorders share the combination of congenital muscular dystrophy and brain malformations including a neuronal migration defect: muscle-eye-brain disease (MEB), Walker-Warburg syndrome (WWS), and Fukuyama congenital muscular dystrophy (FCMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP473696.RAAasbQuhcK_PcD3w6zhFs6SrtjIn-mrAvpRgTkBOUBXY130_provenance.
- NP500320.RAbYguqgFPsY19bVZfYjw4l8wXWjyok-98AGH3L1GsiDE130_assertion description "[Three rare autosomal recessive disorders share the combination of congenital muscular dystrophy and brain malformations including a neuronal migration defect: muscle-eye-brain disease (MEB), Walker-Warburg syndrome (WWS), and Fukuyama congenital muscular dystrophy (FCMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500320.RAbYguqgFPsY19bVZfYjw4l8wXWjyok-98AGH3L1GsiDE130_provenance.
- NP505181.RAZgpwBECzOGGC_tF1XpkXx6Vrbc7XcTTVHcNrTxG-S7k130_assertion description "[Three rare autosomal recessive disorders share the combination of congenital muscular dystrophy and brain malformations including a neuronal migration defect: muscle-eye-brain disease (MEB), Walker-Warburg syndrome (WWS), and Fukuyama congenital muscular dystrophy (FCMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP505181.RAZgpwBECzOGGC_tF1XpkXx6Vrbc7XcTTVHcNrTxG-S7k130_provenance.
- NP835753.RAQjV8S-8yZVwRNuwTdxya0CK9J_zmkdo7gJIc2rK1sbo130_assertion description "[Three rare autosomal recessive disorders share the combination of congenital muscular dystrophy and brain malformations including a neuronal migration defect: muscle-eye-brain disease (MEB), Walker-Warburg syndrome (WWS), and Fukuyama congenital muscular dystrophy (FCMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835753.RAQjV8S-8yZVwRNuwTdxya0CK9J_zmkdo7gJIc2rK1sbo130_provenance.
- NP806518.RA9E80sAXoayvM_cubLiBGUoa60fm5VX6eROCe5DOixZU130_assertion description "[Three rare autosomal recessive disorders share the combination of congenital muscular dystrophy and brain malformations including a neuronal migration defect: muscle-eye-brain disease (MEB), Walker-Warburg syndrome (WWS), and Fukuyama congenital muscular dystrophy (FCMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP806518.RA9E80sAXoayvM_cubLiBGUoa60fm5VX6eROCe5DOixZU130_provenance.
- NP831531.RAa_Z-aCbYKr3hbRpo-IAUpjOgGwxhUE4ZNZ0Aoxli6wQ130_assertion description "[Three rare autosomal recessive disorders share the combination of congenital muscular dystrophy and brain malformations including a neuronal migration defect: muscle-eye-brain disease (MEB), Walker-Warburg syndrome (WWS), and Fukuyama congenital muscular dystrophy (FCMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831531.RAa_Z-aCbYKr3hbRpo-IAUpjOgGwxhUE4ZNZ0Aoxli6wQ130_provenance.
- NP315896.RAQP4NxnalM3ANrjJ9Tqsd1kPdl04m8pATPAQvmLIdKjA130_assertion description "[Three rare autosomal recessive disorders share the combination of congenital muscular dystrophy and brain malformations including a neuronal migration defect: muscle-eye-brain disease (MEB), Walker-Warburg syndrome (WWS), and Fukuyama congenital muscular dystrophy (FCMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP315896.RAQP4NxnalM3ANrjJ9Tqsd1kPdl04m8pATPAQvmLIdKjA130_provenance.
- NP315893.RAnd43SzVg9Z8o35AfpVYj53ToMnTtpcgKOWGWuBEjjO0130_assertion description "[Three rare autosomal recessive disorders share the combination of congenital muscular dystrophy and brain malformations including a neuronal migration defect: muscle-eye-brain disease (MEB), Walker-Warburg syndrome (WWS), and Fukuyama congenital muscular dystrophy (FCMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP315893.RAnd43SzVg9Z8o35AfpVYj53ToMnTtpcgKOWGWuBEjjO0130_provenance.
- NP831568.RAq_EpdAS2GG6jpOlu7v0OaV0qgem1UkWHpDJPcAPdk0M130_assertion description "[Three rare autosomal recessive disorders share the combination of congenital muscular dystrophy and brain malformations including a neuronal migration defect: muscle-eye-brain disease (MEB), Walker-Warburg syndrome (WWS), and Fukuyama congenital muscular dystrophy (FCMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831568.RAq_EpdAS2GG6jpOlu7v0OaV0qgem1UkWHpDJPcAPdk0M130_provenance.
- NP831588.RAGFLKw4hrMWYRMmaA1982fH1GnhiIuL6Qfe8bidzaz9U130_assertion description "[Three rare autosomal recessive disorders share the combination of congenital muscular dystrophy and brain malformations including a neuronal migration defect: muscle-eye-brain disease (MEB), Walker-Warburg syndrome (WWS), and Fukuyama congenital muscular dystrophy (FCMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831588.RAGFLKw4hrMWYRMmaA1982fH1GnhiIuL6Qfe8bidzaz9U130_provenance.
- NP315894.RAE3PemRjz2QUButCA5GLhVKfpXWfViKURRoLGuHEiRsE130_assertion description "[Three rare autosomal recessive disorders share the combination of congenital muscular dystrophy and brain malformations including a neuronal migration defect: muscle-eye-brain disease (MEB), Walker-Warburg syndrome (WWS), and Fukuyama congenital muscular dystrophy (FCMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP315894.RAE3PemRjz2QUButCA5GLhVKfpXWfViKURRoLGuHEiRsE130_provenance.