Matches in Nanopublications for { ?s ?p "[In order to better characterize the phenotypic spectrum associated with FGF3 mutations, we sequenced the FGF3 gene in 10 unrelated families in which probands had congenital deafness associated with various inner ear anomalies, including Michel aplasia, with or without tooth or external ear anomalies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[In order to better characterize the phenotypic spectrum associated with FGF3 mutations, we sequenced the FGF3 gene in 10 unrelated families in which probands had congenital deafness associated with various inner ear anomalies, including Michel aplasia, with or without tooth or external ear anomalies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP399152.RA6PbrGj1XR8clQbazZFWXpC0M8QcniE5EQNZgmGId67g130_assertion description "[In order to better characterize the phenotypic spectrum associated with FGF3 mutations, we sequenced the FGF3 gene in 10 unrelated families in which probands had congenital deafness associated with various inner ear anomalies, including Michel aplasia, with or without tooth or external ear anomalies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP399152.RA6PbrGj1XR8clQbazZFWXpC0M8QcniE5EQNZgmGId67g130_provenance.
- NP667711.RAOT1h3WwIGTxIsep014OsrZX2J4Zn_J08m0cVV8mmUTg130_assertion description "[In order to better characterize the phenotypic spectrum associated with FGF3 mutations, we sequenced the FGF3 gene in 10 unrelated families in which probands had congenital deafness associated with various inner ear anomalies, including Michel aplasia, with or without tooth or external ear anomalies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP667711.RAOT1h3WwIGTxIsep014OsrZX2J4Zn_J08m0cVV8mmUTg130_provenance.