Matches in Nanopublications for { ?s ?p "[Mutations in the transcription factor gene SOX18 cause vascular, lymphatic and hair follicle defects in humans with dominant and recessive forms of hypotrichosis-lymphedema-telangiectasia (HLT) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP437315.RADaAJ9he9-PdZqzFxdeP5jVh38xOAALBTltXrs3zsRJA130_assertion description "[Mutations in the transcription factor gene SOX18 cause vascular, lymphatic and hair follicle defects in humans with dominant and recessive forms of hypotrichosis-lymphedema-telangiectasia (HLT) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP437315.RADaAJ9he9-PdZqzFxdeP5jVh38xOAALBTltXrs3zsRJA130_provenance.
- NP300892.RAEd1mlftkbvTqD-DPJgB6u_IWDlV11bz9YPuZxy5cGNc130_assertion description "[Mutations in the transcription factor gene SOX18 cause vascular, lymphatic and hair follicle defects in humans with dominant and recessive forms of hypotrichosis-lymphedema-telangiectasia (HLT) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP300892.RAEd1mlftkbvTqD-DPJgB6u_IWDlV11bz9YPuZxy5cGNc130_provenance.
- NP910627.RATGXhBKXPPzw-K19BA1IUgAHz3DRBUcSZkzVbBiQwKgc130_assertion description "[Mutations in the transcription factor gene SOX18 cause vascular, lymphatic and hair follicle defects in humans with dominant and recessive forms of hypotrichosis-lymphedema-telangiectasia (HLT) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP910627.RATGXhBKXPPzw-K19BA1IUgAHz3DRBUcSZkzVbBiQwKgc130_provenance.
- assertion description "[Mutations in the transcription factor gene SOX18 cause vascular, lymphatic and hair follicle defects in humans with dominant and recessive forms of hypotrichosis-lymphedema-telangiectasia (HLT) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in the transcription factor gene SOX18 cause vascular, lymphatic and hair follicle defects in humans with dominant and recessive forms of hypotrichosis-lymphedema-telangiectasia (HLT) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP910618.RAixuftrLCttYPmmxrjnU8kEkyAtzTZw-zY4CNPU2X-AA130_assertion description "[Mutations in the transcription factor gene SOX18 cause vascular, lymphatic and hair follicle defects in humans with dominant and recessive forms of hypotrichosis-lymphedema-telangiectasia (HLT) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP910618.RAixuftrLCttYPmmxrjnU8kEkyAtzTZw-zY4CNPU2X-AA130_provenance.
- NP737807.RAjbJof28fg1wJPe6abwLz9UzqCZdw2psK1P4AdprW7eU130_assertion description "[Mutations in the transcription factor gene SOX18 cause vascular, lymphatic and hair follicle defects in humans with dominant and recessive forms of hypotrichosis-lymphedema-telangiectasia (HLT) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP737807.RAjbJof28fg1wJPe6abwLz9UzqCZdw2psK1P4AdprW7eU130_provenance.
- NP737805.RA6IvyY59rWJ6GdGxHE_Xat6aXa5SFcXcjHXSUwZ_E6lg130_assertion description "[Mutations in the transcription factor gene SOX18 cause vascular, lymphatic and hair follicle defects in humans with dominant and recessive forms of hypotrichosis-lymphedema-telangiectasia (HLT) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP737805.RA6IvyY59rWJ6GdGxHE_Xat6aXa5SFcXcjHXSUwZ_E6lg130_provenance.