Matches in Nanopublications for { ?s ?p "[Absence of mutations in NR2E1 and SNX3 in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP300385.RAW3S5-wsS8D996XYFm_z5WnVb9SPiawW45HxOO4mistc130_assertion description "[Absence of mutations in NR2E1 and SNX3 in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP300385.RAW3S5-wsS8D996XYFm_z5WnVb9SPiawW45HxOO4mistc130_provenance.
- NP555008.RAygp7ETUL-5M0_kQjVNaTn5lEIQKhjTFvHUnaJ26dpdY130_assertion description "[Absence of mutations in NR2E1 and SNX3 in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP555008.RAygp7ETUL-5M0_kQjVNaTn5lEIQKhjTFvHUnaJ26dpdY130_provenance.
- NP383633.RAJspfKgVF6fuGdRS4TbQeWpSw7zISqc8WoJX8VY_CBSQ130_assertion description "[Absence of mutations in NR2E1 and SNX3 in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP383633.RAJspfKgVF6fuGdRS4TbQeWpSw7zISqc8WoJX8VY_CBSQ130_provenance.
- NP802651.RAfCR-7rUud_oHkPYED8T17qOxW5rEOpgzaPf1fwmD5xI130_assertion description "[Absence of mutations in NR2E1 and SNX3 in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802651.RAfCR-7rUud_oHkPYED8T17qOxW5rEOpgzaPf1fwmD5xI130_provenance.
- NP802654.RAT-w2X2bd61HlHQwSmVo-mFwHJ_XJzLG3egn79TVaHRg130_assertion description "[Absence of mutations in NR2E1 and SNX3 in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802654.RAT-w2X2bd61HlHQwSmVo-mFwHJ_XJzLG3egn79TVaHRg130_provenance.
- NP621948.RAM8oO7O0nlAaL82GKoHcmd50xBAySmymZUecltQVeyQs130_assertion description "[Absence of mutations in NR2E1 and SNX3 in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP621948.RAM8oO7O0nlAaL82GKoHcmd50xBAySmymZUecltQVeyQs130_provenance.
- NP621947.RA6dmh8buvPm2B8PKKaQpfYenV7FyTtbMGxBX6bAvP9AY130_assertion description "[Absence of mutations in NR2E1 and SNX3 in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP621947.RA6dmh8buvPm2B8PKKaQpfYenV7FyTtbMGxBX6bAvP9AY130_provenance.