Matches in Nanopublications for { ?s ?p "[Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP4556.RACzfDC7nrpWnDlc3V-Z5l9nHKebVEPIPL8wEAW921jDY130_assertion description "[Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4556.RACzfDC7nrpWnDlc3V-Z5l9nHKebVEPIPL8wEAW921jDY130_provenance.
- assertion description "[Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1057100.RAQEf4zU_EV76sE56aTNwV2kc_x0ea98keIVaQSketUSc130_assertion description "[Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1057100.RAQEf4zU_EV76sE56aTNwV2kc_x0ea98keIVaQSketUSc130_provenance.
- assertion description "[Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP964134.RAjg6ohrmIGPa66Kijdxtf9TddGTeOUi1aJr0CL3Kwk3k130_assertion description "[Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP964134.RAjg6ohrmIGPa66Kijdxtf9TddGTeOUi1aJr0CL3Kwk3k130_provenance.
- NP7380.RAOSgLuwpeNyp7YOnC81MwdN2M4DnEVuUNaK3b4KXPCLw130_assertion description "[Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7380.RAOSgLuwpeNyp7YOnC81MwdN2M4DnEVuUNaK3b4KXPCLw130_provenance.