Matches in Nanopublications for { ?s ?p "[Nine probands with a firm clinical diagnosis of PWS but who had neither a typical deletion in the PWS region nor UPD(15)mat were investigated for inactivating mutations in 11 genes located in the PWS region, including SNURF and SNRPN, which are associated with the imprinting centre.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP263098.RAAHlO5sVUWyLIL-r-PEq9wWOibbShE3U1TOnEgZWfLfU130_assertion description "[Nine probands with a firm clinical diagnosis of PWS but who had neither a typical deletion in the PWS region nor UPD(15)mat were investigated for inactivating mutations in 11 genes located in the PWS region, including SNURF and SNRPN, which are associated with the imprinting centre.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263098.RAAHlO5sVUWyLIL-r-PEq9wWOibbShE3U1TOnEgZWfLfU130_provenance.
- NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs130_assertion description "[Nine probands with a firm clinical diagnosis of PWS but who had neither a typical deletion in the PWS region nor UPD(15)mat were investigated for inactivating mutations in 11 genes located in the PWS region, including SNURF and SNRPN, which are associated with the imprinting centre.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs130_provenance.
- NP673545.RAbU5gqd6avn_DVy-Z-dRfllqpJxQvnyqAsYWJAzr_IyA130_assertion description "[Nine probands with a firm clinical diagnosis of PWS but who had neither a typical deletion in the PWS region nor UPD(15)mat were investigated for inactivating mutations in 11 genes located in the PWS region, including SNURF and SNRPN, which are associated with the imprinting centre.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP673545.RAbU5gqd6avn_DVy-Z-dRfllqpJxQvnyqAsYWJAzr_IyA130_provenance.
- NP591319.RAdgGVb_cJpYPmpPxiFW-1O5VofD8qoJNPM_3fW8nJuCk130_assertion description "[Nine probands with a firm clinical diagnosis of PWS but who had neither a typical deletion in the PWS region nor UPD(15)mat were investigated for inactivating mutations in 11 genes located in the PWS region, including SNURF and SNRPN, which are associated with the imprinting centre.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP591319.RAdgGVb_cJpYPmpPxiFW-1O5VofD8qoJNPM_3fW8nJuCk130_provenance.
- NP591321.RASNGInruj75L3z4iHoM2OgTO39mCoY4hBFRnTKxtIDp8130_assertion description "[Nine probands with a firm clinical diagnosis of PWS but who had neither a typical deletion in the PWS region nor UPD(15)mat were investigated for inactivating mutations in 11 genes located in the PWS region, including SNURF and SNRPN, which are associated with the imprinting centre.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP591321.RASNGInruj75L3z4iHoM2OgTO39mCoY4hBFRnTKxtIDp8130_provenance.
- NP811449.RAi2sgvDqSCreHntSDSrDDQ5ZNJ9srrcOOMLx-m_XuabI130_assertion description "[Nine probands with a firm clinical diagnosis of PWS but who had neither a typical deletion in the PWS region nor UPD(15)mat were investigated for inactivating mutations in 11 genes located in the PWS region, including SNURF and SNRPN, which are associated with the imprinting centre.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP811449.RAi2sgvDqSCreHntSDSrDDQ5ZNJ9srrcOOMLx-m_XuabI130_provenance.
- NP591322.RAHBMgl7-8GpvcQpzH6RXUiJLM4EvVJHoB_-vt8gL13dQ130_assertion description "[Nine probands with a firm clinical diagnosis of PWS but who had neither a typical deletion in the PWS region nor UPD(15)mat were investigated for inactivating mutations in 11 genes located in the PWS region, including SNURF and SNRPN, which are associated with the imprinting centre.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP591322.RAHBMgl7-8GpvcQpzH6RXUiJLM4EvVJHoB_-vt8gL13dQ130_provenance.
- NP767214.RA_VSgtB0MtSYkJMC8ZTr7Lote3A7kFWiGoeKtrCDZwIs130_assertion description "[Nine probands with a firm clinical diagnosis of PWS but who had neither a typical deletion in the PWS region nor UPD(15)mat were investigated for inactivating mutations in 11 genes located in the PWS region, including SNURF and SNRPN, which are associated with the imprinting centre.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767214.RA_VSgtB0MtSYkJMC8ZTr7Lote3A7kFWiGoeKtrCDZwIs130_provenance.