Matches in Nanopublications for { ?s ?p "[Heterozygosity for mutations in the TGFBR1 or TGFBR2 genes cause Loeys-Dietz syndrome (LDS) types 2A and 2B that overlap with MFS1 in their clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP529850.RAw7QGDGXDT7jfTolMFdoSOotwrZUkadL7sam_Nd32O1Q130_assertion description "[Heterozygosity for mutations in the TGFBR1 or TGFBR2 genes cause Loeys-Dietz syndrome (LDS) types 2A and 2B that overlap with MFS1 in their clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP529850.RAw7QGDGXDT7jfTolMFdoSOotwrZUkadL7sam_Nd32O1Q130_provenance.
- NP734060.RAXelxirc6bD51gioiykR8qhJARtfgWOpgZun_O3o2Q1Y130_assertion description "[Heterozygosity for mutations in the TGFBR1 or TGFBR2 genes cause Loeys-Dietz syndrome (LDS) types 2A and 2B that overlap with MFS1 in their clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734060.RAXelxirc6bD51gioiykR8qhJARtfgWOpgZun_O3o2Q1Y130_provenance.
- assertion description "[Heterozygosity for mutations in the TGFBR1 or TGFBR2 genes cause Loeys-Dietz syndrome (LDS) types 2A and 2B that overlap with MFS1 in their clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Heterozygosity for mutations in the TGFBR1 or TGFBR2 genes cause Loeys-Dietz syndrome (LDS) types 2A and 2B that overlap with MFS1 in their clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Heterozygosity for mutations in the TGFBR1 or TGFBR2 genes cause Loeys-Dietz syndrome (LDS) types 2A and 2B that overlap with MFS1 in their clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Heterozygosity for mutations in the TGFBR1 or TGFBR2 genes cause Loeys-Dietz syndrome (LDS) types 2A and 2B that overlap with MFS1 in their clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP715831.RAXA-bwXacL2Sat_HjLS8P_dA4-xJX4s9xfBDcI71-xQA130_assertion description "[Heterozygosity for mutations in the TGFBR1 or TGFBR2 genes cause Loeys-Dietz syndrome (LDS) types 2A and 2B that overlap with MFS1 in their clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715831.RAXA-bwXacL2Sat_HjLS8P_dA4-xJX4s9xfBDcI71-xQA130_provenance.
- NP734443.RAwSG2VBJFIPEDJopUBPX88f94Xb7UbsejvlyD2eNC3qs130_assertion description "[Heterozygosity for mutations in the TGFBR1 or TGFBR2 genes cause Loeys-Dietz syndrome (LDS) types 2A and 2B that overlap with MFS1 in their clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734443.RAwSG2VBJFIPEDJopUBPX88f94Xb7UbsejvlyD2eNC3qs130_provenance.
- NP715829.RAxMlJI_S5gCinF2uWr8-V2ZugH6Gyrvzeokg9ha4QlQI130_assertion description "[Heterozygosity for mutations in the TGFBR1 or TGFBR2 genes cause Loeys-Dietz syndrome (LDS) types 2A and 2B that overlap with MFS1 in their clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715829.RAxMlJI_S5gCinF2uWr8-V2ZugH6Gyrvzeokg9ha4QlQI130_provenance.
- NP715830.RAx_E-sl-yRyidMzqgTMYTBJfh0jQLNVS6kp0IiMSOw0U130_assertion description "[Heterozygosity for mutations in the TGFBR1 or TGFBR2 genes cause Loeys-Dietz syndrome (LDS) types 2A and 2B that overlap with MFS1 in their clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715830.RAx_E-sl-yRyidMzqgTMYTBJfh0jQLNVS6kp0IiMSOw0U130_provenance.
- NP715833.RA915uqmsjTZ9xM3KoUZHgBd_VW4PpzePFJZH42ybSUcQ130_assertion description "[Heterozygosity for mutations in the TGFBR1 or TGFBR2 genes cause Loeys-Dietz syndrome (LDS) types 2A and 2B that overlap with MFS1 in their clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715833.RA915uqmsjTZ9xM3KoUZHgBd_VW4PpzePFJZH42ybSUcQ130_provenance.