Matches in Nanopublications for { ?s ?p "[Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP368255.RAUiKorlx3QqfKVOEz2_rBEhXre52y_7oFW41iMM3oCCg130_assertion description "[Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP368255.RAUiKorlx3QqfKVOEz2_rBEhXre52y_7oFW41iMM3oCCg130_provenance.
- NP7249.RAT9ywMyUIFvn_fLyC4Fm0TNt_K_qc7hLyHudUcCHH_Kw130_assertion description "[Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7249.RAT9ywMyUIFvn_fLyC4Fm0TNt_K_qc7hLyHudUcCHH_Kw130_provenance.
- NP1020659.RAaikpX5II9kMoN2k2pr8wH08ozquVeXw6kPfIz5N7Wxw130_assertion description "[Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1020659.RAaikpX5II9kMoN2k2pr8wH08ozquVeXw6kPfIz5N7Wxw130_provenance.
- NP4003.RAO4dE8TRKV9VBqc-qGa38tXWHUrn8d1DuNfySy2J_FvI130_assertion description "[Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4003.RAO4dE8TRKV9VBqc-qGa38tXWHUrn8d1DuNfySy2J_FvI130_provenance.
- NP1020655.RAj849fllb12MzPf6rKdCpEu5o9zmujJ9eP5MlK7p6o4Q130_assertion description "[Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1020655.RAj849fllb12MzPf6rKdCpEu5o9zmujJ9eP5MlK7p6o4Q130_provenance.
- NP1020657.RAvh6Y6yXgcR1iPXvqHtVxw-73wR9IqO2612X6rqtxmPI130_assertion description "[Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1020657.RAvh6Y6yXgcR1iPXvqHtVxw-73wR9IqO2612X6rqtxmPI130_provenance.
- NP368248.RA9fsvceRfnDJoKAnylmpFtN-mo4ozFmyq6V-vAatNI8Y130_assertion description "[Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP368248.RA9fsvceRfnDJoKAnylmpFtN-mo4ozFmyq6V-vAatNI8Y130_provenance.
- NP368254.RAHdiOSAvprwOLufryX4uHc0e8mIGx8NX2t3C2o-xSXBk130_assertion description "[Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP368254.RAHdiOSAvprwOLufryX4uHc0e8mIGx8NX2t3C2o-xSXBk130_provenance.
- NP368256.RAE-aKlINfcJ6lRQzVnTwbSM8lU7mXOinLK1ZtguXNEGc130_assertion description "[Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP368256.RAE-aKlINfcJ6lRQzVnTwbSM8lU7mXOinLK1ZtguXNEGc130_provenance.