Matches in Nanopublications for { ?s ?p "[Taken together, these findings suggest that autosomal genes account for the majority of familial cases of KS, and that unique neuroendocrine phenotypes consistent with some GnRH neuronal migration may exist in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_assertion description "[Taken together, these findings suggest that autosomal genes account for the majority of familial cases of KS, and that unique neuroendocrine phenotypes consistent with some GnRH neuronal migration may exist in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_provenance.
- NP314017.RAV7BRUsoOdzU1RHxHT_3wVV8bKVnofKvgf8DIaZhMZBw130_assertion description "[Taken together, these findings suggest that autosomal genes account for the majority of familial cases of KS, and that unique neuroendocrine phenotypes consistent with some GnRH neuronal migration may exist in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP314017.RAV7BRUsoOdzU1RHxHT_3wVV8bKVnofKvgf8DIaZhMZBw130_provenance.
- NP831504.RAsPDQDdYv46WMgH6kmzr2pDx_Zd9Kx1qJg9-nMO9ipT4130_assertion description "[Taken together, these findings suggest that autosomal genes account for the majority of familial cases of KS, and that unique neuroendocrine phenotypes consistent with some GnRH neuronal migration may exist in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831504.RAsPDQDdYv46WMgH6kmzr2pDx_Zd9Kx1qJg9-nMO9ipT4130_provenance.