Matches in Nanopublications for { ?s ?p "[The 14 additional phenotypes (84 patients: 46%) included PNH with Ehlers-Danlos syndrome (EDS), temporo-occipital PNH with hippocampal malformation and cerebellar hypoplasia, PNH with fronto-perisylvian or temporo-occipital polymicrogyria, posterior PNH with hydrocephalus, PNH with microcephaly, PNH with frontonasal dysplasia, PNH with limb abnormalities, PNH with fragile-X syndrome, PNH with ambiguous genitalia, micronodular PH, unilateral PNH, laminar ribbon-like and linear PH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP263717.RAfYuWU9hDWqvf4UA5XCmLtMY_RRwIHGP7mrjghSw_aAs130_assertion description "[The 14 additional phenotypes (84 patients: 46%) included PNH with Ehlers-Danlos syndrome (EDS), temporo-occipital PNH with hippocampal malformation and cerebellar hypoplasia, PNH with fronto-perisylvian or temporo-occipital polymicrogyria, posterior PNH with hydrocephalus, PNH with microcephaly, PNH with frontonasal dysplasia, PNH with limb abnormalities, PNH with fragile-X syndrome, PNH with ambiguous genitalia, micronodular PH, unilateral PNH, laminar ribbon-like and linear PH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263717.RAfYuWU9hDWqvf4UA5XCmLtMY_RRwIHGP7mrjghSw_aAs130_provenance.
- NP380906.RAnjPa1pfHZ5ukCw-GSC0rVmf9woQ8PPVyOP9JCNaACSs130_assertion description "[The 14 additional phenotypes (84 patients: 46%) included PNH with Ehlers-Danlos syndrome (EDS), temporo-occipital PNH with hippocampal malformation and cerebellar hypoplasia, PNH with fronto-perisylvian or temporo-occipital polymicrogyria, posterior PNH with hydrocephalus, PNH with microcephaly, PNH with frontonasal dysplasia, PNH with limb abnormalities, PNH with fragile-X syndrome, PNH with ambiguous genitalia, micronodular PH, unilateral PNH, laminar ribbon-like and linear PH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP380906.RAnjPa1pfHZ5ukCw-GSC0rVmf9woQ8PPVyOP9JCNaACSs130_provenance.
- NP817712.RAo5PyJ-q0EtW2-gXB8AWm1vLbPn7rahNbt7sAohVL2F8130_assertion description "[The 14 additional phenotypes (84 patients: 46%) included PNH with Ehlers-Danlos syndrome (EDS), temporo-occipital PNH with hippocampal malformation and cerebellar hypoplasia, PNH with fronto-perisylvian or temporo-occipital polymicrogyria, posterior PNH with hydrocephalus, PNH with microcephaly, PNH with frontonasal dysplasia, PNH with limb abnormalities, PNH with fragile-X syndrome, PNH with ambiguous genitalia, micronodular PH, unilateral PNH, laminar ribbon-like and linear PH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP817712.RAo5PyJ-q0EtW2-gXB8AWm1vLbPn7rahNbt7sAohVL2F8130_provenance.
- NP672320.RAf0C8IARP9ATYh3KmEYzN_V9n9oSPA4j_nD6jEvj62TE130_assertion description "[The 14 additional phenotypes (84 patients: 46%) included PNH with Ehlers-Danlos syndrome (EDS), temporo-occipital PNH with hippocampal malformation and cerebellar hypoplasia, PNH with fronto-perisylvian or temporo-occipital polymicrogyria, posterior PNH with hydrocephalus, PNH with microcephaly, PNH with frontonasal dysplasia, PNH with limb abnormalities, PNH with fragile-X syndrome, PNH with ambiguous genitalia, micronodular PH, unilateral PNH, laminar ribbon-like and linear PH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP672320.RAf0C8IARP9ATYh3KmEYzN_V9n9oSPA4j_nD6jEvj62TE130_provenance.
- NP579915.RAfm_3W_6M0sR7s4uf8XdalELnG-yzC9dwYt_uaJXS0Qk130_assertion description "[The 14 additional phenotypes (84 patients: 46%) included PNH with Ehlers-Danlos syndrome (EDS), temporo-occipital PNH with hippocampal malformation and cerebellar hypoplasia, PNH with fronto-perisylvian or temporo-occipital polymicrogyria, posterior PNH with hydrocephalus, PNH with microcephaly, PNH with frontonasal dysplasia, PNH with limb abnormalities, PNH with fragile-X syndrome, PNH with ambiguous genitalia, micronodular PH, unilateral PNH, laminar ribbon-like and linear PH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP579915.RAfm_3W_6M0sR7s4uf8XdalELnG-yzC9dwYt_uaJXS0Qk130_provenance.
- NP857676.RA8x355Alc2kX83X4D5_6izLr-La7DqQZlxeOlhjDGIwo130_assertion description "[The 14 additional phenotypes (84 patients: 46%) included PNH with Ehlers-Danlos syndrome (EDS), temporo-occipital PNH with hippocampal malformation and cerebellar hypoplasia, PNH with fronto-perisylvian or temporo-occipital polymicrogyria, posterior PNH with hydrocephalus, PNH with microcephaly, PNH with frontonasal dysplasia, PNH with limb abnormalities, PNH with fragile-X syndrome, PNH with ambiguous genitalia, micronodular PH, unilateral PNH, laminar ribbon-like and linear PH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP857676.RA8x355Alc2kX83X4D5_6izLr-La7DqQZlxeOlhjDGIwo130_provenance.
- NP545716.RAOPv_vHSOQ8mXslNZJhSnEya4ZQIxOQuZBqcaQDax804130_assertion description "[The 14 additional phenotypes (84 patients: 46%) included PNH with Ehlers-Danlos syndrome (EDS), temporo-occipital PNH with hippocampal malformation and cerebellar hypoplasia, PNH with fronto-perisylvian or temporo-occipital polymicrogyria, posterior PNH with hydrocephalus, PNH with microcephaly, PNH with frontonasal dysplasia, PNH with limb abnormalities, PNH with fragile-X syndrome, PNH with ambiguous genitalia, micronodular PH, unilateral PNH, laminar ribbon-like and linear PH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP545716.RAOPv_vHSOQ8mXslNZJhSnEya4ZQIxOQuZBqcaQDax804130_provenance.