Matches in Nanopublications for { ?s ?p "[Mutation analysis of the ALX4 gene in three unrelated FPP families without the MSX2 mutation identified mutations in two families, indicating that mutations in ALX4 could be responsible for these skull defects and suggesting further genetic heterogeneity of FPP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Mutation analysis of the ALX4 gene in three unrelated FPP families without the MSX2 mutation identified mutations in two families, indicating that mutations in ALX4 could be responsible for these skull defects and suggesting further genetic heterogeneity of FPP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP302228.RABZoc-Q-CYRnuUHuYXqy3LD-9AhCUENtYOI0UYukkYXg130_assertion description "[Mutation analysis of the ALX4 gene in three unrelated FPP families without the MSX2 mutation identified mutations in two families, indicating that mutations in ALX4 could be responsible for these skull defects and suggesting further genetic heterogeneity of FPP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP302228.RABZoc-Q-CYRnuUHuYXqy3LD-9AhCUENtYOI0UYukkYXg130_provenance.
- NP571845.RAOEFhwBdgmQHgrbCoFSK6JmoBqIqy2H5Sj-lTDZj0el8130_assertion description "[Mutation analysis of the ALX4 gene in three unrelated FPP families without the MSX2 mutation identified mutations in two families, indicating that mutations in ALX4 could be responsible for these skull defects and suggesting further genetic heterogeneity of FPP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP571845.RAOEFhwBdgmQHgrbCoFSK6JmoBqIqy2H5Sj-lTDZj0el8130_provenance.