Matches in Nanopublications for { ?s ?p "[Mutations in MECP2 cause classic or preserved speech variant Rett syndrome and intellectual disability in females and early demise or marked neurodevelopmental handicap in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP805222.RATfydhcoq2vjKSDb8dfR2hIrA3TL0uWkqCM_RC0nVW0Q130_assertion description "[Mutations in MECP2 cause classic or preserved speech variant Rett syndrome and intellectual disability in females and early demise or marked neurodevelopmental handicap in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP805222.RATfydhcoq2vjKSDb8dfR2hIrA3TL0uWkqCM_RC0nVW0Q130_provenance.
- NP702064.RAASSRpqRblS-TeoxV5KODJVkEh8tbVL02td-mbUZwA48130_assertion description "[Mutations in MECP2 cause classic or preserved speech variant Rett syndrome and intellectual disability in females and early demise or marked neurodevelopmental handicap in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP702064.RAASSRpqRblS-TeoxV5KODJVkEh8tbVL02td-mbUZwA48130_provenance.
- NP552234.RAaUsan6aMYGf181E-IcCAwR7QxQcqSklpAmyBJ3KgDZU130_assertion description "[Mutations in MECP2 cause classic or preserved speech variant Rett syndrome and intellectual disability in females and early demise or marked neurodevelopmental handicap in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP552234.RAaUsan6aMYGf181E-IcCAwR7QxQcqSklpAmyBJ3KgDZU130_provenance.
- NP552197.RANmS42UVDKWjfSn2sAqNU1w08CHk0TT0o_U2iu0ZLEdc130_assertion description "[Mutations in MECP2 cause classic or preserved speech variant Rett syndrome and intellectual disability in females and early demise or marked neurodevelopmental handicap in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP552197.RANmS42UVDKWjfSn2sAqNU1w08CHk0TT0o_U2iu0ZLEdc130_provenance.
- NP702065.RASNZcnlAo-NB8aKqcyVIp3ukcRm-pzEtKJCVxKQDmMVU130_assertion description "[Mutations in MECP2 cause classic or preserved speech variant Rett syndrome and intellectual disability in females and early demise or marked neurodevelopmental handicap in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP702065.RASNZcnlAo-NB8aKqcyVIp3ukcRm-pzEtKJCVxKQDmMVU130_provenance.
- assertion description "[Mutations in MECP2 cause classic or preserved speech variant Rett syndrome and intellectual disability in females and early demise or marked neurodevelopmental handicap in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in MECP2 cause classic or preserved speech variant Rett syndrome and intellectual disability in females and early demise or marked neurodevelopmental handicap in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.