Matches in Nanopublications for { ?s ?p "[We characterized a deletion distal to the DMRT genes in a patient with isolated 46,XY gonadal DSD and narrowed down the breakpoint in a patient with a 46,XY del(9)(p23) karyotype with gonadal DSD and mild symptoms of 9p deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP401609.RA25jb4E_kdc8ubbLjCpL3a8_R24x4sSXSgEAJM8eiv5M130_assertion description "[We characterized a deletion distal to the DMRT genes in a patient with isolated 46,XY gonadal DSD and narrowed down the breakpoint in a patient with a 46,XY del(9)(p23) karyotype with gonadal DSD and mild symptoms of 9p deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401609.RA25jb4E_kdc8ubbLjCpL3a8_R24x4sSXSgEAJM8eiv5M130_provenance.
- NP717763.RAKrETvmOQ-F-IAnlJuYvYJPj7dd5T4MIExmedQ5-AgR4130_assertion description "[We characterized a deletion distal to the DMRT genes in a patient with isolated 46,XY gonadal DSD and narrowed down the breakpoint in a patient with a 46,XY del(9)(p23) karyotype with gonadal DSD and mild symptoms of 9p deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP717763.RAKrETvmOQ-F-IAnlJuYvYJPj7dd5T4MIExmedQ5-AgR4130_provenance.
- NP658905.RAHCpCxE-PHYJqgjY2tbuD3CW-ov-UiCqCTTUnIAllrwA130_assertion description "[We characterized a deletion distal to the DMRT genes in a patient with isolated 46,XY gonadal DSD and narrowed down the breakpoint in a patient with a 46,XY del(9)(p23) karyotype with gonadal DSD and mild symptoms of 9p deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP658905.RAHCpCxE-PHYJqgjY2tbuD3CW-ov-UiCqCTTUnIAllrwA130_provenance.
- NP705197.RA0w7DteS91za7wuaydAu73gSsprDmlfeGXzatQuWj28Y130_assertion description "[We characterized a deletion distal to the DMRT genes in a patient with isolated 46,XY gonadal DSD and narrowed down the breakpoint in a patient with a 46,XY del(9)(p23) karyotype with gonadal DSD and mild symptoms of 9p deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP705197.RA0w7DteS91za7wuaydAu73gSsprDmlfeGXzatQuWj28Y130_provenance.
- NP883186.RAHHsg-5OSbqWvSgRYh1OQIo8oW76AhZM0oo-B_XEJqLg130_assertion description "[We characterized a deletion distal to the DMRT genes in a patient with isolated 46,XY gonadal DSD and narrowed down the breakpoint in a patient with a 46,XY del(9)(p23) karyotype with gonadal DSD and mild symptoms of 9p deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP883186.RAHHsg-5OSbqWvSgRYh1OQIo8oW76AhZM0oo-B_XEJqLg130_provenance.