Matches in Nanopublications for { ?s ?p "[Deletion 11(p11.2p12) is a rare, yet specific, deletion syndrome involving the EXT2 locus, a gene for parietal foramina, and a mental retardation locus, and therefore can be classified as a contiguous gene deletion syndrome.]. 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.
- NP822309.RAfEnMOb-QK92cPm12EVgxFDSRUFM1--2bhD5uoZm5QLs130_assertion description "[Deletion 11(p11.2p12) is a rare, yet specific, deletion syndrome involving the EXT2 locus, a gene for parietal foramina, and a mental retardation locus, and therefore can be classified as a contiguous gene deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP822309.RAfEnMOb-QK92cPm12EVgxFDSRUFM1--2bhD5uoZm5QLs130_provenance.
- NP736835.RAA6ZtK9Uqtzz7psSQxN3peh0knMeLIZKF8jez1FT9_80130_assertion description "[Deletion 11(p11.2p12) is a rare, yet specific, deletion syndrome involving the EXT2 locus, a gene for parietal foramina, and a mental retardation locus, and therefore can be classified as a contiguous gene deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP736835.RAA6ZtK9Uqtzz7psSQxN3peh0knMeLIZKF8jez1FT9_80130_provenance.
- NP464844.RA8LBwjNOe6Vk7s2XVYNJ_LxRy-d3_u_5XLprJZaGAX9U130_assertion description "[Deletion 11(p11.2p12) is a rare, yet specific, deletion syndrome involving the EXT2 locus, a gene for parietal foramina, and a mental retardation locus, and therefore can be classified as a contiguous gene deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP464844.RA8LBwjNOe6Vk7s2XVYNJ_LxRy-d3_u_5XLprJZaGAX9U130_provenance.
- NP592626.RA4FlKHiNMpdipNs0mJ_1N7LUT3DxB5JCz0zKxNAWK1-8130_assertion description "[Deletion 11(p11.2p12) is a rare, yet specific, deletion syndrome involving the EXT2 locus, a gene for parietal foramina, and a mental retardation locus, and therefore can be classified as a contiguous gene deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP592626.RA4FlKHiNMpdipNs0mJ_1N7LUT3DxB5JCz0zKxNAWK1-8130_provenance.
- NP460649.RAuflrUlrre26jIVdklFeaEEZen7Ps74IDSI3K-L5bL2k130_assertion description "[Deletion 11(p11.2p12) is a rare, yet specific, deletion syndrome involving the EXT2 locus, a gene for parietal foramina, and a mental retardation locus, and therefore can be classified as a contiguous gene deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP460649.RAuflrUlrre26jIVdklFeaEEZen7Ps74IDSI3K-L5bL2k130_provenance.
- NP697136.RAIHx1mhDZ57gXLn4eohS81fWKlZ-ac6TFpdtHZm1cMjI130_assertion description "[Deletion 11(p11.2p12) is a rare, yet specific, deletion syndrome involving the EXT2 locus, a gene for parietal foramina, and a mental retardation locus, and therefore can be classified as a contiguous gene deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697136.RAIHx1mhDZ57gXLn4eohS81fWKlZ-ac6TFpdtHZm1cMjI130_provenance.