Matches in Nanopublications for { ?s ?p "[DAX1 mutations were found in 58% (37 of 64) of 46,XY phenotypic boys referred with adrenal hypoplasia and in all boys (eight of eight) with hypogonadotropic hypogonadism and a family history suggestive of adrenal failure in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[DAX1 mutations were found in 58% (37 of 64) of 46,XY phenotypic boys referred with adrenal hypoplasia and in all boys (eight of eight) with hypogonadotropic hypogonadism and a family history suggestive of adrenal failure in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[DAX1 mutations were found in 58% (37 of 64) of 46,XY phenotypic boys referred with adrenal hypoplasia and in all boys (eight of eight) with hypogonadotropic hypogonadism and a family history suggestive of adrenal failure in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP231090.RAXgmaFJIyrKO5m9CF3eFoc4gR_m2iuLeaD62hzZH7rmE130_assertion description "[DAX1 mutations were found in 58% (37 of 64) of 46,XY phenotypic boys referred with adrenal hypoplasia and in all boys (eight of eight) with hypogonadotropic hypogonadism and a family history suggestive of adrenal failure in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP231090.RAXgmaFJIyrKO5m9CF3eFoc4gR_m2iuLeaD62hzZH7rmE130_provenance.
- NP548846.RASAAAC9CEuyqwNuQIs_uME3qmDtaPaAVcMOoEFebwFWU130_assertion description "[DAX1 mutations were found in 58% (37 of 64) of 46,XY phenotypic boys referred with adrenal hypoplasia and in all boys (eight of eight) with hypogonadotropic hypogonadism and a family history suggestive of adrenal failure in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP548846.RASAAAC9CEuyqwNuQIs_uME3qmDtaPaAVcMOoEFebwFWU130_provenance.
- NP548847.RAZePpwQG5Dbt-4uEiKm8P8cwxQ59BX08K-JO20Wb0oj4130_assertion description "[DAX1 mutations were found in 58% (37 of 64) of 46,XY phenotypic boys referred with adrenal hypoplasia and in all boys (eight of eight) with hypogonadotropic hypogonadism and a family history suggestive of adrenal failure in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP548847.RAZePpwQG5Dbt-4uEiKm8P8cwxQ59BX08K-JO20Wb0oj4130_provenance.
- NP548850.RAV-aeSNNieRhSZ6qTW2GuYZlSGnz3n7t8Ykqxp2XphKI130_assertion description "[DAX1 mutations were found in 58% (37 of 64) of 46,XY phenotypic boys referred with adrenal hypoplasia and in all boys (eight of eight) with hypogonadotropic hypogonadism and a family history suggestive of adrenal failure in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP548850.RAV-aeSNNieRhSZ6qTW2GuYZlSGnz3n7t8Ykqxp2XphKI130_provenance.
- NP548848.RA38DFe1Z6wv0cPgc7r0MJVHozV-JYauqqYQQVlFXRCCg130_assertion description "[DAX1 mutations were found in 58% (37 of 64) of 46,XY phenotypic boys referred with adrenal hypoplasia and in all boys (eight of eight) with hypogonadotropic hypogonadism and a family history suggestive of adrenal failure in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP548848.RA38DFe1Z6wv0cPgc7r0MJVHozV-JYauqqYQQVlFXRCCg130_provenance.