Matches in Nanopublications for { ?s ?p "[Heterozygous mutations in the FGFR1 gene accompanied by a high frequency of cleft palate and other facial dysmorphisms were recently identified in 8% of a large KS cohort, yet the reproductive phenotype of KS patients harboring FGFR1 mutations has not been described.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP261608.RATlT3lqbcfZKBxA0T-bJSllulpTTIdIvepobhuTGLYbE130_assertion description "[Heterozygous mutations in the FGFR1 gene accompanied by a high frequency of cleft palate and other facial dysmorphisms were recently identified in 8% of a large KS cohort, yet the reproductive phenotype of KS patients harboring FGFR1 mutations has not been described.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261608.RATlT3lqbcfZKBxA0T-bJSllulpTTIdIvepobhuTGLYbE130_provenance.
- NP249754.RAkluBKQBLVX-6T2pBCjrSaezUBsovIHym8lJxr2osjVU130_assertion description "[Heterozygous mutations in the FGFR1 gene accompanied by a high frequency of cleft palate and other facial dysmorphisms were recently identified in 8% of a large KS cohort, yet the reproductive phenotype of KS patients harboring FGFR1 mutations has not been described.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP249754.RAkluBKQBLVX-6T2pBCjrSaezUBsovIHym8lJxr2osjVU130_provenance.
- assertion description "[Heterozygous mutations in the FGFR1 gene accompanied by a high frequency of cleft palate and other facial dysmorphisms were recently identified in 8% of a large KS cohort, yet the reproductive phenotype of KS patients harboring FGFR1 mutations has not been described.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Heterozygous mutations in the FGFR1 gene accompanied by a high frequency of cleft palate and other facial dysmorphisms were recently identified in 8% of a large KS cohort, yet the reproductive phenotype of KS patients harboring FGFR1 mutations has not been described.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Heterozygous mutations in the FGFR1 gene accompanied by a high frequency of cleft palate and other facial dysmorphisms were recently identified in 8% of a large KS cohort, yet the reproductive phenotype of KS patients harboring FGFR1 mutations has not been described.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.