Matches in Nanopublications for { ?s ?p "[Snyder-Robinson syndrome (SRS, OMIM 309583) is a rare X-linked syndrome characterized by mental retardation, marfanoid habitus, skeletal defects, osteoporosis, and facial asymmetry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP924337.RACwqiEyBUiIZHiuCp8t63dXpCNnUaSloB7yjr3UaYg6Y130_assertion description "[Snyder-Robinson syndrome (SRS, OMIM 309583) is a rare X-linked syndrome characterized by mental retardation, marfanoid habitus, skeletal defects, osteoporosis, and facial asymmetry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924337.RACwqiEyBUiIZHiuCp8t63dXpCNnUaSloB7yjr3UaYg6Y130_provenance.
- NP251028.RAoVG0IIOucQgnJ8Ixe3DnWDAJnvCYsiRhWuuyHH2U9sk130_assertion description "[Snyder-Robinson syndrome (SRS, OMIM 309583) is a rare X-linked syndrome characterized by mental retardation, marfanoid habitus, skeletal defects, osteoporosis, and facial asymmetry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP251028.RAoVG0IIOucQgnJ8Ixe3DnWDAJnvCYsiRhWuuyHH2U9sk130_provenance.
- NP764158.RAareO-SQCC6g8gSy7x4KJcAPhiLdtCC1GQbgXoA7YADU130_assertion description "[Snyder-Robinson syndrome (SRS, OMIM 309583) is a rare X-linked syndrome characterized by mental retardation, marfanoid habitus, skeletal defects, osteoporosis, and facial asymmetry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP764158.RAareO-SQCC6g8gSy7x4KJcAPhiLdtCC1GQbgXoA7YADU130_provenance.
- NP568483.RA-WGjJ80onUSeVM-A1pt21iE2Kv3A9pTiisUQsX-6rMg130_assertion description "[Snyder-Robinson syndrome (SRS, OMIM 309583) is a rare X-linked syndrome characterized by mental retardation, marfanoid habitus, skeletal defects, osteoporosis, and facial asymmetry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568483.RA-WGjJ80onUSeVM-A1pt21iE2Kv3A9pTiisUQsX-6rMg130_provenance.
- NP312693.RAHbMbNSm6eOQ1300y0Nu6KqoeLc5NynrPlflqPL2drxE130_assertion description "[Snyder-Robinson syndrome (SRS, OMIM 309583) is a rare X-linked syndrome characterized by mental retardation, marfanoid habitus, skeletal defects, osteoporosis, and facial asymmetry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP312693.RAHbMbNSm6eOQ1300y0Nu6KqoeLc5NynrPlflqPL2drxE130_provenance.
- NP683792.RAJkJZL2YlFTjGf39JCT634JJoPybn_6iMwBqevEiSj10130_assertion description "[Snyder-Robinson syndrome (SRS, OMIM 309583) is a rare X-linked syndrome characterized by mental retardation, marfanoid habitus, skeletal defects, osteoporosis, and facial asymmetry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683792.RAJkJZL2YlFTjGf39JCT634JJoPybn_6iMwBqevEiSj10130_provenance.
- NP866962.RAJP3D8NXB0iiw1-6bpbSBGiNlmgDyA-syOLz-87k8C_Y130_assertion description "[Snyder-Robinson syndrome (SRS, OMIM 309583) is a rare X-linked syndrome characterized by mental retardation, marfanoid habitus, skeletal defects, osteoporosis, and facial asymmetry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP866962.RAJP3D8NXB0iiw1-6bpbSBGiNlmgDyA-syOLz-87k8C_Y130_provenance.