Matches in Nanopublications for { ?s ?p "[Such rare CDKN1B variants may contribute to the development of pituitary adenomas, but their low incidence and lack of clear segregation with affected patients make CDKN1B sequencing unlikely to be of use in routine genetic investigation of FIPA kindreds.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP303392.RAvDa15CK8qljcI9cMnass-Mj-YShMhKR204D3XJjcwyU130_assertion description "[Such rare CDKN1B variants may contribute to the development of pituitary adenomas, but their low incidence and lack of clear segregation with affected patients make CDKN1B sequencing unlikely to be of use in routine genetic investigation of FIPA kindreds.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP303392.RAvDa15CK8qljcI9cMnass-Mj-YShMhKR204D3XJjcwyU130_provenance.
- NP957233.RAk_YAjC1Zw3Qy2SoTEXm-RjQrumBqv7I6Sy4CmkCrq20130_assertion description "[Such rare CDKN1B variants may contribute to the development of pituitary adenomas, but their low incidence and lack of clear segregation with affected patients make CDKN1B sequencing unlikely to be of use in routine genetic investigation of FIPA kindreds.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP957233.RAk_YAjC1Zw3Qy2SoTEXm-RjQrumBqv7I6Sy4CmkCrq20130_provenance.