Matches in Nanopublications for { ?s ?p "[Here, we report five heterozygous NOTCH1 variants in unrelated individuals with Adams-Oliver syndrome (AOS), a rare disease with major features of aplasia cutis of the scalp and terminal transverse limb defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP595581.RAfvp_mPv2YpbOWh1FdpFpDM2MJFNr1qrZkLf_1PPQLWY130_assertion description "[Here, we report five heterozygous NOTCH1 variants in unrelated individuals with Adams-Oliver syndrome (AOS), a rare disease with major features of aplasia cutis of the scalp and terminal transverse limb defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP595581.RAfvp_mPv2YpbOWh1FdpFpDM2MJFNr1qrZkLf_1PPQLWY130_provenance.
- NP595717.RAZnz2U9N6ouxXlEOghky_FeQ6hvjZZZzadCckqHJzUi4130_assertion description "[Here, we report five heterozygous NOTCH1 variants in unrelated individuals with Adams-Oliver syndrome (AOS), a rare disease with major features of aplasia cutis of the scalp and terminal transverse limb defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP595717.RAZnz2U9N6ouxXlEOghky_FeQ6hvjZZZzadCckqHJzUi4130_provenance.
- assertion description "[Here, we report five heterozygous NOTCH1 variants in unrelated individuals with Adams-Oliver syndrome (AOS), a rare disease with major features of aplasia cutis of the scalp and terminal transverse limb defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Here, we report five heterozygous NOTCH1 variants in unrelated individuals with Adams-Oliver syndrome (AOS), a rare disease with major features of aplasia cutis of the scalp and terminal transverse limb defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1211570.RAkS40squIf73925OdYswjdJ4kEWVu8za1ZAlUpz1vELo130_assertion description "[Here, we report five heterozygous NOTCH1 variants in unrelated individuals with Adams-Oliver syndrome (AOS), a rare disease with major features of aplasia cutis of the scalp and terminal transverse limb defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1211570.RAkS40squIf73925OdYswjdJ4kEWVu8za1ZAlUpz1vELo130_provenance.
- NP595606.RA_PDSvOs1BzKXnYBANSGlkqq6wZ-e-QLXdORo8DR-m5k130_assertion description "[Here, we report five heterozygous NOTCH1 variants in unrelated individuals with Adams-Oliver syndrome (AOS), a rare disease with major features of aplasia cutis of the scalp and terminal transverse limb defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP595606.RA_PDSvOs1BzKXnYBANSGlkqq6wZ-e-QLXdORo8DR-m5k130_provenance.
- NP1211572.RAPMTJpff61QzCd5O7BnBu6-yHGlmTx34ZetQYTssoGgU130_assertion description "[Here, we report five heterozygous NOTCH1 variants in unrelated individuals with Adams-Oliver syndrome (AOS), a rare disease with major features of aplasia cutis of the scalp and terminal transverse limb defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1211572.RAPMTJpff61QzCd5O7BnBu6-yHGlmTx34ZetQYTssoGgU130_provenance.