Matches in Nanopublications for { ?s ?p "[The TBX1 gene is considered to be the major candidate gene for the main features in 22q11.2 deletion syndrome, including congenital heart malformations, (para)thyroid hypoplasia, and craniofacial abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 13 of
13
with 100 items per page.
- NP724396.RAdAhPI7DbYmP5zVceYAVdspn-YI-ywYr-D8Hx_JAFIXs130_assertion description "[The TBX1 gene is considered to be the major candidate gene for the main features in 22q11.2 deletion syndrome, including congenital heart malformations, (para)thyroid hypoplasia, and craniofacial abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724396.RAdAhPI7DbYmP5zVceYAVdspn-YI-ywYr-D8Hx_JAFIXs130_provenance.
- NP300844.RAmMYBMozWTyXMC0F1VL0I9im5ILrXCR3Nrs1f1Hzmo5s130_assertion description "[The TBX1 gene is considered to be the major candidate gene for the main features in 22q11.2 deletion syndrome, including congenital heart malformations, (para)thyroid hypoplasia, and craniofacial abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP300844.RAmMYBMozWTyXMC0F1VL0I9im5ILrXCR3Nrs1f1Hzmo5s130_provenance.
- NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_assertion description "[The TBX1 gene is considered to be the major candidate gene for the main features in 22q11.2 deletion syndrome, including congenital heart malformations, (para)thyroid hypoplasia, and craniofacial abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_provenance.
- assertion description "[The TBX1 gene is considered to be the major candidate gene for the main features in 22q11.2 deletion syndrome, including congenital heart malformations, (para)thyroid hypoplasia, and craniofacial abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The TBX1 gene is considered to be the major candidate gene for the main features in 22q11.2 deletion syndrome, including congenital heart malformations, (para)thyroid hypoplasia, and craniofacial abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1005251.RAdo4eotUa9DhwYzx1SXSOCUp7WzSe3SL_J9LDv6JqyW0130_assertion description "[The TBX1 gene is considered to be the major candidate gene for the main features in 22q11.2 deletion syndrome, including congenital heart malformations, (para)thyroid hypoplasia, and craniofacial abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1005251.RAdo4eotUa9DhwYzx1SXSOCUp7WzSe3SL_J9LDv6JqyW0130_provenance.
- NP1005248.RADl_8ZvvFIcxfxLTNEURdEpevPUQJVobI_IIq9VxZ4bM130_assertion description "[The TBX1 gene is considered to be the major candidate gene for the main features in 22q11.2 deletion syndrome, including congenital heart malformations, (para)thyroid hypoplasia, and craniofacial abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1005248.RADl_8ZvvFIcxfxLTNEURdEpevPUQJVobI_IIq9VxZ4bM130_provenance.
- NP723451.RAEvUGAfPJTRs_IXnb5OwYNpvVagVBcGBzZa3bv2zq82I130_assertion description "[The TBX1 gene is considered to be the major candidate gene for the main features in 22q11.2 deletion syndrome, including congenital heart malformations, (para)thyroid hypoplasia, and craniofacial abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723451.RAEvUGAfPJTRs_IXnb5OwYNpvVagVBcGBzZa3bv2zq82I130_provenance.
- NP1005247.RAOMXBqx1OxJnUxdFUdSZ2ZPZ9jZW7Xm5gx96lVxifYNc130_assertion description "[The TBX1 gene is considered to be the major candidate gene for the main features in 22q11.2 deletion syndrome, including congenital heart malformations, (para)thyroid hypoplasia, and craniofacial abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1005247.RAOMXBqx1OxJnUxdFUdSZ2ZPZ9jZW7Xm5gx96lVxifYNc130_provenance.
- NP1005252.RAMNgDVc7RcFZMaOuEyt6kcrIr57Cr4JKynB4yUpnlVpg130_assertion description "[The TBX1 gene is considered to be the major candidate gene for the main features in 22q11.2 deletion syndrome, including congenital heart malformations, (para)thyroid hypoplasia, and craniofacial abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1005252.RAMNgDVc7RcFZMaOuEyt6kcrIr57Cr4JKynB4yUpnlVpg130_provenance.
- NP723307.RAwCPKR1ZtxBx1w7Hw3x7_b6s6W3pJ47CZq9A8y1VIjjs130_assertion description "[The TBX1 gene is considered to be the major candidate gene for the main features in 22q11.2 deletion syndrome, including congenital heart malformations, (para)thyroid hypoplasia, and craniofacial abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723307.RAwCPKR1ZtxBx1w7Hw3x7_b6s6W3pJ47CZq9A8y1VIjjs130_provenance.
- NP723325.RAzEp5SaimoZProS7EqHp5CwQxiFvdrUUA5fLlDGqfdJc130_assertion description "[The TBX1 gene is considered to be the major candidate gene for the main features in 22q11.2 deletion syndrome, including congenital heart malformations, (para)thyroid hypoplasia, and craniofacial abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723325.RAzEp5SaimoZProS7EqHp5CwQxiFvdrUUA5fLlDGqfdJc130_provenance.
- NP723405.RA8AYGpI0kyrO-7lX5jIqYNwj4iBao7cWmAcKPlj2aj2c130_assertion description "[The TBX1 gene is considered to be the major candidate gene for the main features in 22q11.2 deletion syndrome, including congenital heart malformations, (para)thyroid hypoplasia, and craniofacial abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723405.RA8AYGpI0kyrO-7lX5jIqYNwj4iBao7cWmAcKPlj2aj2c130_provenance.