Matches in Nanopublications for { ?s ?p "[Hemihypertrophy is also reported as part of the Beckwith-Wiedemann syndrome which has as its cardinal features omphalocele, macroglossia and gigantism with hypoglycemia, organomegaly, renal anomalies, hemihypertrophy, and embryonal tumors occurring less frequently.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP625995.RAlWkqsAcgQm1xQE8KQFJMphUhlay3NBbDQl3hgh_kdS0130_assertion description "[Hemihypertrophy is also reported as part of the Beckwith-Wiedemann syndrome which has as its cardinal features omphalocele, macroglossia and gigantism with hypoglycemia, organomegaly, renal anomalies, hemihypertrophy, and embryonal tumors occurring less frequently.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP625995.RAlWkqsAcgQm1xQE8KQFJMphUhlay3NBbDQl3hgh_kdS0130_provenance.
- NP321884.RA-hrCFgeEwslIQ5S8Ywgkbjk_jPW2zWlbFA14ixJq2js130_assertion description "[Hemihypertrophy is also reported as part of the Beckwith-Wiedemann syndrome which has as its cardinal features omphalocele, macroglossia and gigantism with hypoglycemia, organomegaly, renal anomalies, hemihypertrophy, and embryonal tumors occurring less frequently.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321884.RA-hrCFgeEwslIQ5S8Ywgkbjk_jPW2zWlbFA14ixJq2js130_provenance.
- NP586054.RAa-qk9aTib2QT1dYDfRhRpZb-8Fwn2EEOw8vHCMYFds8130_assertion description "[Hemihypertrophy is also reported as part of the Beckwith-Wiedemann syndrome which has as its cardinal features omphalocele, macroglossia and gigantism with hypoglycemia, organomegaly, renal anomalies, hemihypertrophy, and embryonal tumors occurring less frequently.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP586054.RAa-qk9aTib2QT1dYDfRhRpZb-8Fwn2EEOw8vHCMYFds8130_provenance.
- NP865126.RA58iud47x5fKv3-LKCaBiZ5rUVtkGPKHYSWm43kO1FUY130_assertion description "[Hemihypertrophy is also reported as part of the Beckwith-Wiedemann syndrome which has as its cardinal features omphalocele, macroglossia and gigantism with hypoglycemia, organomegaly, renal anomalies, hemihypertrophy, and embryonal tumors occurring less frequently.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP865126.RA58iud47x5fKv3-LKCaBiZ5rUVtkGPKHYSWm43kO1FUY130_provenance.
- NP1413423.RAAbOQFWRpyMWAfhYR2VoRZd-8qbd5DFg4AGsxM7Lznxg130_assertion description "[Hemihypertrophy is also reported as part of the Beckwith-Wiedemann syndrome which has as its cardinal features omphalocele, macroglossia and gigantism with hypoglycemia, organomegaly, renal anomalies, hemihypertrophy, and embryonal tumors occurring less frequently.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1413423.RAAbOQFWRpyMWAfhYR2VoRZd-8qbd5DFg4AGsxM7Lznxg130_provenance.
- NP1013276.RAM7cNGXgTRl2MOTYAuioRU1vpABzUJNeuFILMBVi-4Ss130_assertion description "[Hemihypertrophy is also reported as part of the Beckwith-Wiedemann syndrome which has as its cardinal features omphalocele, macroglossia and gigantism with hypoglycemia, organomegaly, renal anomalies, hemihypertrophy, and embryonal tumors occurring less frequently.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1013276.RAM7cNGXgTRl2MOTYAuioRU1vpABzUJNeuFILMBVi-4Ss130_provenance.
- NP1013270.RA-oFycewmw6l6PhKP4JOo282T_wzYJwSJXTeBJ-zgYrA130_assertion description "[Hemihypertrophy is also reported as part of the Beckwith-Wiedemann syndrome which has as its cardinal features omphalocele, macroglossia and gigantism with hypoglycemia, organomegaly, renal anomalies, hemihypertrophy, and embryonal tumors occurring less frequently.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1013270.RA-oFycewmw6l6PhKP4JOo282T_wzYJwSJXTeBJ-zgYrA130_provenance.
- NP1413421.RAwQlXfzeS6RR_6TXYyhtBO_lzWipQNHwoJq6LDpdFDns130_assertion description "[Hemihypertrophy is also reported as part of the Beckwith-Wiedemann syndrome which has as its cardinal features omphalocele, macroglossia and gigantism with hypoglycemia, organomegaly, renal anomalies, hemihypertrophy, and embryonal tumors occurring less frequently.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1413421.RAwQlXfzeS6RR_6TXYyhtBO_lzWipQNHwoJq6LDpdFDns130_provenance.