Matches in Nanopublications for { ?s ?p "[An autosomal dominant form of hereditary gingival fibromatosis (HGF, MIM 135300) was recently mapped to chromosome 2p21 in a large Brazilian family and there was an earlier report of GF in a boy with a cytogenetic duplication involving 2p13-->p21.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP262156.RAiV6ZB6gbzNbzquDbhXNtjzw4gEVwg5O2uGco_rAlWbs130_assertion description "[An autosomal dominant form of hereditary gingival fibromatosis (HGF, MIM 135300) was recently mapped to chromosome 2p21 in a large Brazilian family and there was an earlier report of GF in a boy with a cytogenetic duplication involving 2p13-->p21.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262156.RAiV6ZB6gbzNbzquDbhXNtjzw4gEVwg5O2uGco_rAlWbs130_provenance.
- NP596521.RA1-bSvJSpbCBzCVMJu5_KK-xg7QzDzNVprUAPLTTkfws130_assertion description "[An autosomal dominant form of hereditary gingival fibromatosis (HGF, MIM 135300) was recently mapped to chromosome 2p21 in a large Brazilian family and there was an earlier report of GF in a boy with a cytogenetic duplication involving 2p13-->p21.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP596521.RA1-bSvJSpbCBzCVMJu5_KK-xg7QzDzNVprUAPLTTkfws130_provenance.
- NP524384.RAReTKhO-afLtrh4lNcVs9g_NdosnzjojG4mH2aSKDDgE130_assertion description "[An autosomal dominant form of hereditary gingival fibromatosis (HGF, MIM 135300) was recently mapped to chromosome 2p21 in a large Brazilian family and there was an earlier report of GF in a boy with a cytogenetic duplication involving 2p13-->p21.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP524384.RAReTKhO-afLtrh4lNcVs9g_NdosnzjojG4mH2aSKDDgE130_provenance.
- NP435808.RA2_i1Zna20WnGKDLq0vUsVRC9GETnLjsD57xBlS70n5s130_assertion description "[An autosomal dominant form of hereditary gingival fibromatosis (HGF, MIM 135300) was recently mapped to chromosome 2p21 in a large Brazilian family and there was an earlier report of GF in a boy with a cytogenetic duplication involving 2p13-->p21.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP435808.RA2_i1Zna20WnGKDLq0vUsVRC9GETnLjsD57xBlS70n5s130_provenance.