Matches in Nanopublications for { ?s ?p "[The progressive parting of CDKL5- and FOXG1-gene-related encephalopathies from the core Rett syndrome is reflected by the effort to produce clearer diagnostic criteria for typical and atypical Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP258982.RAuvXyEVxpZ6aci6SQul1znlHZ-DFhYs2V1elKfjchff8130_assertion description "[The progressive parting of CDKL5- and FOXG1-gene-related encephalopathies from the core Rett syndrome is reflected by the effort to produce clearer diagnostic criteria for typical and atypical Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258982.RAuvXyEVxpZ6aci6SQul1znlHZ-DFhYs2V1elKfjchff8130_provenance.
- NP807819.RAlYlNKoMqYHhdyaC5Bdba7wq8RelolbGDHC7E7Gb-FXY130_assertion description "[The progressive parting of CDKL5- and FOXG1-gene-related encephalopathies from the core Rett syndrome is reflected by the effort to produce clearer diagnostic criteria for typical and atypical Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP807819.RAlYlNKoMqYHhdyaC5Bdba7wq8RelolbGDHC7E7Gb-FXY130_provenance.
- assertion description "[The progressive parting of CDKL5- and FOXG1-gene-related encephalopathies from the core Rett syndrome is reflected by the effort to produce clearer diagnostic criteria for typical and atypical Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The progressive parting of CDKL5- and FOXG1-gene-related encephalopathies from the core Rett syndrome is reflected by the effort to produce clearer diagnostic criteria for typical and atypical Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP675494.RAxw5bS9zYAin18SdLdj-KVOK7hAx-6OePUzS5I9UnhXw130_assertion description "[The progressive parting of CDKL5- and FOXG1-gene-related encephalopathies from the core Rett syndrome is reflected by the effort to produce clearer diagnostic criteria for typical and atypical Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP675494.RAxw5bS9zYAin18SdLdj-KVOK7hAx-6OePUzS5I9UnhXw130_provenance.
- NP719402.RAYiF_6Ery2eWVHmRu5G79VmBpafrPTyEC2XboFeyW9uk130_assertion description "[The progressive parting of CDKL5- and FOXG1-gene-related encephalopathies from the core Rett syndrome is reflected by the effort to produce clearer diagnostic criteria for typical and atypical Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719402.RAYiF_6Ery2eWVHmRu5G79VmBpafrPTyEC2XboFeyW9uk130_provenance.
- assertion description "[The progressive parting of CDKL5- and FOXG1-gene-related encephalopathies from the core Rett syndrome is reflected by the effort to produce clearer diagnostic criteria for typical and atypical Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1014881.RAXHZMZzBeyQ8yK0xzrOJdOP0UCpabpncOonVC8qQby1g130_assertion description "[The progressive parting of CDKL5- and FOXG1-gene-related encephalopathies from the core Rett syndrome is reflected by the effort to produce clearer diagnostic criteria for typical and atypical Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1014881.RAXHZMZzBeyQ8yK0xzrOJdOP0UCpabpncOonVC8qQby1g130_provenance.
- NP1014879.RAtfKrKSiMjjTmLtyRQ_-Tyt6nwSkan-cIRLpkoQ1gALQ130_assertion description "[The progressive parting of CDKL5- and FOXG1-gene-related encephalopathies from the core Rett syndrome is reflected by the effort to produce clearer diagnostic criteria for typical and atypical Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1014879.RAtfKrKSiMjjTmLtyRQ_-Tyt6nwSkan-cIRLpkoQ1gALQ130_provenance.
- NP404328.RAJhkukKFxggGjnUkM2dIyzoW3s6jf5tbvvuqH-KZlKng130_assertion description "[The progressive parting of CDKL5- and FOXG1-gene-related encephalopathies from the core Rett syndrome is reflected by the effort to produce clearer diagnostic criteria for typical and atypical Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404328.RAJhkukKFxggGjnUkM2dIyzoW3s6jf5tbvvuqH-KZlKng130_provenance.
- NP404356.RAELXVJdL39JENDj_LHpJXZ_-bp449BI_3ljMg4KWqoeM130_assertion description "[The progressive parting of CDKL5- and FOXG1-gene-related encephalopathies from the core Rett syndrome is reflected by the effort to produce clearer diagnostic criteria for typical and atypical Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404356.RAELXVJdL39JENDj_LHpJXZ_-bp449BI_3ljMg4KWqoeM130_provenance.
- NP1014882.RANpZaIOi4TUaR2WRIwYoyjde-yHtqL-eYzRavVg2iloc130_assertion description "[The progressive parting of CDKL5- and FOXG1-gene-related encephalopathies from the core Rett syndrome is reflected by the effort to produce clearer diagnostic criteria for typical and atypical Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1014882.RANpZaIOi4TUaR2WRIwYoyjde-yHtqL-eYzRavVg2iloc130_provenance.
- NP1014878.RA-o2AiREI8aTVFm6qbiD2FW7MsB5cJblB_EkesKvm6sc130_assertion description "[The progressive parting of CDKL5- and FOXG1-gene-related encephalopathies from the core Rett syndrome is reflected by the effort to produce clearer diagnostic criteria for typical and atypical Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1014878.RA-o2AiREI8aTVFm6qbiD2FW7MsB5cJblB_EkesKvm6sc130_provenance.