Matches in Nanopublications for { ?s ?p "[We report here a new family with X-linked mental retardation due to mutation in OPHN1 and present unpublished data about two families previously reported, concerning the facial and psychological phenotype of affected males and carrier females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 4 of
4
with 100 items per page.
- NP197608.RADff5KjcUJkuuyh8lUCThwV3ySsTd3QFDI6hXZe_8BcU130_assertion description "[We report here a new family with X-linked mental retardation due to mutation in OPHN1 and present unpublished data about two families previously reported, concerning the facial and psychological phenotype of affected males and carrier females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP197608.RADff5KjcUJkuuyh8lUCThwV3ySsTd3QFDI6hXZe_8BcU130_provenance.
- assertion description "[We report here a new family with X-linked mental retardation due to mutation in OPHN1 and present unpublished data about two families previously reported, concerning the facial and psychological phenotype of affected males and carrier females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP603248.RAD1wIgEjc84uV1Sco11ad2hU1EEVKDQdU2sx4O5ngNeY130_assertion description "[We report here a new family with X-linked mental retardation due to mutation in OPHN1 and present unpublished data about two families previously reported, concerning the facial and psychological phenotype of affected males and carrier females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP603248.RAD1wIgEjc84uV1Sco11ad2hU1EEVKDQdU2sx4O5ngNeY130_provenance.
- NP513181.RApgxSaRVm9kBCv4GEtpscAUl48F88c9LQO04DSNOmeEI130_assertion description "[We report here a new family with X-linked mental retardation due to mutation in OPHN1 and present unpublished data about two families previously reported, concerning the facial and psychological phenotype of affected males and carrier females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP513181.RApgxSaRVm9kBCv4GEtpscAUl48F88c9LQO04DSNOmeEI130_provenance.