Matches in Nanopublications for { ?s ?p "[Our study clearly demonstrated that recurrent c.1938delC in ITGB4 is a founder mutation in JEB-PA patients, and that genotyping of the mutation can be utilized for prenatal diagnosis of JEB-PA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP668175.RAgvtSqbHLfDYISbjxjmh2PytoVRIK8zGDA0cTLWK1ms4130_assertion description "[Our study clearly demonstrated that recurrent c.1938delC in ITGB4 is a founder mutation in JEB-PA patients, and that genotyping of the mutation can be utilized for prenatal diagnosis of JEB-PA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668175.RAgvtSqbHLfDYISbjxjmh2PytoVRIK8zGDA0cTLWK1ms4130_provenance.
- NP518143.RATEhdIEE-KlU3qY69h18XMjnCu4fGnrdk_uyohzJ8p00130_assertion description "[Our study clearly demonstrated that recurrent c.1938delC in ITGB4 is a founder mutation in JEB-PA patients, and that genotyping of the mutation can be utilized for prenatal diagnosis of JEB-PA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP518143.RATEhdIEE-KlU3qY69h18XMjnCu4fGnrdk_uyohzJ8p00130_provenance.
- assertion description "[Our study clearly demonstrated that recurrent c.1938delC in ITGB4 is a founder mutation in JEB-PA patients, and that genotyping of the mutation can be utilized for prenatal diagnosis of JEB-PA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP846433.RA7NxJuL0AzVwmLCcGD7MBs6K5jluDwmES8S6gtaqcwCA130_assertion description "[Our study clearly demonstrated that recurrent c.1938delC in ITGB4 is a founder mutation in JEB-PA patients, and that genotyping of the mutation can be utilized for prenatal diagnosis of JEB-PA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP846433.RA7NxJuL0AzVwmLCcGD7MBs6K5jluDwmES8S6gtaqcwCA130_provenance.