Matches in Nanopublications for { ?s ?p "[Fragile X syndrome is the most common form of inherited mental retardation currently known, associated with a wide range of developmental disabilities in both males and females, caused by a large expansion of a (CGG)n repeat in the first exon of the FMR1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP483578.RAJbrjIROy2tcHp4oHIJniC74tr2mDagA8g0Az0PRvhFY130_assertion description "[Fragile X syndrome is the most common form of inherited mental retardation currently known, associated with a wide range of developmental disabilities in both males and females, caused by a large expansion of a (CGG)n repeat in the first exon of the FMR1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP483578.RAJbrjIROy2tcHp4oHIJniC74tr2mDagA8g0Az0PRvhFY130_provenance.
- NP677778.RALpHJetWyZt-Dl9RVuPgkrZj4fdOrJI31VRN45Dt_AM4130_assertion description "[Fragile X syndrome is the most common form of inherited mental retardation currently known, associated with a wide range of developmental disabilities in both males and females, caused by a large expansion of a (CGG)n repeat in the first exon of the FMR1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP677778.RALpHJetWyZt-Dl9RVuPgkrZj4fdOrJI31VRN45Dt_AM4130_provenance.
- NP253475.RABjCNUN9hshexqOCJGIZYrj-3zfV7pIGX1GCsD5yNvOY130_assertion description "[Fragile X syndrome is the most common form of inherited mental retardation currently known, associated with a wide range of developmental disabilities in both males and females, caused by a large expansion of a (CGG)n repeat in the first exon of the FMR1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP253475.RABjCNUN9hshexqOCJGIZYrj-3zfV7pIGX1GCsD5yNvOY130_provenance.
- NP412421.RAaEzBDlXNI8MPv3oHcM-gwwhRFYE8ffDIs6fqQaqUHJo130_assertion description "[Fragile X syndrome is the most common form of inherited mental retardation currently known, associated with a wide range of developmental disabilities in both males and females, caused by a large expansion of a (CGG)n repeat in the first exon of the FMR1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412421.RAaEzBDlXNI8MPv3oHcM-gwwhRFYE8ffDIs6fqQaqUHJo130_provenance.
- assertion description "[Fragile X syndrome is the most common form of inherited mental retardation currently known, associated with a wide range of developmental disabilities in both males and females, caused by a large expansion of a (CGG)n repeat in the first exon of the FMR1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP253474.RA2W98QToHyALPEjPtfEAgv8MQVSRXj0vgV-IIs6XuQls130_assertion description "[Fragile X syndrome is the most common form of inherited mental retardation currently known, associated with a wide range of developmental disabilities in both males and females, caused by a large expansion of a (CGG)n repeat in the first exon of the FMR1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP253474.RA2W98QToHyALPEjPtfEAgv8MQVSRXj0vgV-IIs6XuQls130_provenance.
- NP408690.RANckCyPhPPHM55VwTc6RoacyClGk_Pb0LzydSo_4hu4g130_assertion description "[Fragile X syndrome is the most common form of inherited mental retardation currently known, associated with a wide range of developmental disabilities in both males and females, caused by a large expansion of a (CGG)n repeat in the first exon of the FMR1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408690.RANckCyPhPPHM55VwTc6RoacyClGk_Pb0LzydSo_4hu4g130_provenance.
- NP253472.RAnlzA-o0Rs647TLBhXIv5oCQDXv3XLqHuAEfR6ai578w130_assertion description "[Fragile X syndrome is the most common form of inherited mental retardation currently known, associated with a wide range of developmental disabilities in both males and females, caused by a large expansion of a (CGG)n repeat in the first exon of the FMR1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP253472.RAnlzA-o0Rs647TLBhXIv5oCQDXv3XLqHuAEfR6ai578w130_provenance.
- NP253476.RAvmfkVD1c9innqitYJB62MVuhVyGHGVUzmEbaMnUVmqU130_assertion description "[Fragile X syndrome is the most common form of inherited mental retardation currently known, associated with a wide range of developmental disabilities in both males and females, caused by a large expansion of a (CGG)n repeat in the first exon of the FMR1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP253476.RAvmfkVD1c9innqitYJB62MVuhVyGHGVUzmEbaMnUVmqU130_provenance.