Matches in Nanopublications for { ?s ?p "[Infrequently, FBN1 mutations cause dominantly inherited Weill-Marchesani syndrome (WMS), isolated ectopia lentis (IEL), or the fibrotic condition, geleophysic dysplasia (GD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP609180.RAs7Q8bjajPW_RZ-JcILFUcafjihHXOar_00oSDx385us130_assertion description "[Infrequently, FBN1 mutations cause dominantly inherited Weill-Marchesani syndrome (WMS), isolated ectopia lentis (IEL), or the fibrotic condition, geleophysic dysplasia (GD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP609180.RAs7Q8bjajPW_RZ-JcILFUcafjihHXOar_00oSDx385us130_provenance.
- NP846167.RApKm6ikuUJH3Qz4ntSJy-08imABLmVkTwMhLvx4uxwxg130_assertion description "[Infrequently, FBN1 mutations cause dominantly inherited Weill-Marchesani syndrome (WMS), isolated ectopia lentis (IEL), or the fibrotic condition, geleophysic dysplasia (GD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP846167.RApKm6ikuUJH3Qz4ntSJy-08imABLmVkTwMhLvx4uxwxg130_provenance.
- assertion description "[Infrequently, FBN1 mutations cause dominantly inherited Weill-Marchesani syndrome (WMS), isolated ectopia lentis (IEL), or the fibrotic condition, geleophysic dysplasia (GD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Infrequently, FBN1 mutations cause dominantly inherited Weill-Marchesani syndrome (WMS), isolated ectopia lentis (IEL), or the fibrotic condition, geleophysic dysplasia (GD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Infrequently, FBN1 mutations cause dominantly inherited Weill-Marchesani syndrome (WMS), isolated ectopia lentis (IEL), or the fibrotic condition, geleophysic dysplasia (GD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP458988.RA0M5Imp8BSDGNQnnFjfBHrTOXgLophtCvJI0prWl3Lvc130_assertion description "[Infrequently, FBN1 mutations cause dominantly inherited Weill-Marchesani syndrome (WMS), isolated ectopia lentis (IEL), or the fibrotic condition, geleophysic dysplasia (GD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP458988.RA0M5Imp8BSDGNQnnFjfBHrTOXgLophtCvJI0prWl3Lvc130_provenance.
- NP639454.RAGWdwYlGAQ1Kb_dl-kvW4-1NuQDlvaJtwiqvZwOsHpJc130_assertion description "[Infrequently, FBN1 mutations cause dominantly inherited Weill-Marchesani syndrome (WMS), isolated ectopia lentis (IEL), or the fibrotic condition, geleophysic dysplasia (GD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP639454.RAGWdwYlGAQ1Kb_dl-kvW4-1NuQDlvaJtwiqvZwOsHpJc130_provenance.
- NP395927.RAHPpFIsHmrqaJmk4_mt34dRb55rql_R0OeBOXbh0qCuI130_assertion description "[Infrequently, FBN1 mutations cause dominantly inherited Weill-Marchesani syndrome (WMS), isolated ectopia lentis (IEL), or the fibrotic condition, geleophysic dysplasia (GD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP395927.RAHPpFIsHmrqaJmk4_mt34dRb55rql_R0OeBOXbh0qCuI130_provenance.
- NP918453.RA-ByTW9ggn4U6HxbPz2QPNV5YKDi2P_qwTRQPG2zReOc130_assertion description "[Infrequently, FBN1 mutations cause dominantly inherited Weill-Marchesani syndrome (WMS), isolated ectopia lentis (IEL), or the fibrotic condition, geleophysic dysplasia (GD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP918453.RA-ByTW9ggn4U6HxbPz2QPNV5YKDi2P_qwTRQPG2zReOc130_provenance.