Matches in Nanopublications for { ?s ?p "[A deletion of at least 11.5 cM in the paternal X chromosome mapping between microsatellites DXS989 and DXS1003 and encompassing the genes for ornithine transcarbamylase (OTC), retinitis pigmentosa GTPase regulator (RPGR) and dystrophin, was associated with the loss of band Xp21 in a female patient with OTC deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP619076.RABWq6_NLQr07By50KzKlQvK7lSMZxESYTzuVAr53Cfpk130_assertion description "[A deletion of at least 11.5 cM in the paternal X chromosome mapping between microsatellites DXS989 and DXS1003 and encompassing the genes for ornithine transcarbamylase (OTC), retinitis pigmentosa GTPase regulator (RPGR) and dystrophin, was associated with the loss of band Xp21 in a female patient with OTC deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP619076.RABWq6_NLQr07By50KzKlQvK7lSMZxESYTzuVAr53Cfpk130_provenance.
- assertion description "[A deletion of at least 11.5 cM in the paternal X chromosome mapping between microsatellites DXS989 and DXS1003 and encompassing the genes for ornithine transcarbamylase (OTC), retinitis pigmentosa GTPase regulator (RPGR) and dystrophin, was associated with the loss of band Xp21 in a female patient with OTC deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[A deletion of at least 11.5 cM in the paternal X chromosome mapping between microsatellites DXS989 and DXS1003 and encompassing the genes for ornithine transcarbamylase (OTC), retinitis pigmentosa GTPase regulator (RPGR) and dystrophin, was associated with the loss of band Xp21 in a female patient with OTC deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP355491.RAv4e80A3UyFoSIliNHJ9G661nOSUQ9412Efg-7hu_rKU130_assertion description "[A deletion of at least 11.5 cM in the paternal X chromosome mapping between microsatellites DXS989 and DXS1003 and encompassing the genes for ornithine transcarbamylase (OTC), retinitis pigmentosa GTPase regulator (RPGR) and dystrophin, was associated with the loss of band Xp21 in a female patient with OTC deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355491.RAv4e80A3UyFoSIliNHJ9G661nOSUQ9412Efg-7hu_rKU130_provenance.
- NP674513.RADaqSR1TjQ25MGE3ay8iJQ3FcwrXZFXbX6RM8WLLhGY4130_assertion description "[A deletion of at least 11.5 cM in the paternal X chromosome mapping between microsatellites DXS989 and DXS1003 and encompassing the genes for ornithine transcarbamylase (OTC), retinitis pigmentosa GTPase regulator (RPGR) and dystrophin, was associated with the loss of band Xp21 in a female patient with OTC deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674513.RADaqSR1TjQ25MGE3ay8iJQ3FcwrXZFXbX6RM8WLLhGY4130_provenance.
- NP264338.RAne4hvMEuBiykiQ35DlxfkducqhkNccTnUDlZjysnoR4130_assertion description "[A deletion of at least 11.5 cM in the paternal X chromosome mapping between microsatellites DXS989 and DXS1003 and encompassing the genes for ornithine transcarbamylase (OTC), retinitis pigmentosa GTPase regulator (RPGR) and dystrophin, was associated with the loss of band Xp21 in a female patient with OTC deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP264338.RAne4hvMEuBiykiQ35DlxfkducqhkNccTnUDlZjysnoR4130_provenance.
- NP894146.RAORnh_19POmqXTZaf9mYJyx1ZimJRMx8_9uT2Hf37xxY130_assertion description "[A deletion of at least 11.5 cM in the paternal X chromosome mapping between microsatellites DXS989 and DXS1003 and encompassing the genes for ornithine transcarbamylase (OTC), retinitis pigmentosa GTPase regulator (RPGR) and dystrophin, was associated with the loss of band Xp21 in a female patient with OTC deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP894146.RAORnh_19POmqXTZaf9mYJyx1ZimJRMx8_9uT2Hf37xxY130_provenance.
- NP264339.RANmVSq51PavbTGP8jkwqdPg9p8a8zedd6-JvcxcwYCRE130_assertion description "[A deletion of at least 11.5 cM in the paternal X chromosome mapping between microsatellites DXS989 and DXS1003 and encompassing the genes for ornithine transcarbamylase (OTC), retinitis pigmentosa GTPase regulator (RPGR) and dystrophin, was associated with the loss of band Xp21 in a female patient with OTC deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP264339.RANmVSq51PavbTGP8jkwqdPg9p8a8zedd6-JvcxcwYCRE130_provenance.