Matches in Nanopublications for { ?s ?p "[Lack of NPHP2 mutations in a newborn infant with Joubert syndrome-related disorder presenting as end-stage renal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 9 of
9
with 100 items per page.
- NP194034.RA6EezTd7YmDeXcxWErCSDNQ4He0LmebV7nsoVdeRikUw130_assertion description "[Lack of NPHP2 mutations in a newborn infant with Joubert syndrome-related disorder presenting as end-stage renal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP194034.RA6EezTd7YmDeXcxWErCSDNQ4He0LmebV7nsoVdeRikUw130_provenance.
- NP719717.RAMPePTARpHEAP2JVnv9jjZg5EljC9_cquzAJfMeNveWw130_assertion description "[Lack of NPHP2 mutations in a newborn infant with Joubert syndrome-related disorder presenting as end-stage renal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719717.RAMPePTARpHEAP2JVnv9jjZg5EljC9_cquzAJfMeNveWw130_provenance.
- NP588238.RADAWpvVIJoy9ZvVNwd270hMxCd0fYy9uqnFt8AJ4OHUo130_assertion description "[Lack of NPHP2 mutations in a newborn infant with Joubert syndrome-related disorder presenting as end-stage renal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588238.RADAWpvVIJoy9ZvVNwd270hMxCd0fYy9uqnFt8AJ4OHUo130_provenance.
- NP886222.RAeOcD2VfwxKyTpQF7RAzZbv8nD0s2KYwQgdn4SBaFRXs130_assertion description "[Lack of NPHP2 mutations in a newborn infant with Joubert syndrome-related disorder presenting as end-stage renal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886222.RAeOcD2VfwxKyTpQF7RAzZbv8nD0s2KYwQgdn4SBaFRXs130_provenance.
- NP588237.RA6ut48su7-RSqPWBbfICSBYfRUKZA29WhViqzPn0OC_g130_assertion description "[Lack of NPHP2 mutations in a newborn infant with Joubert syndrome-related disorder presenting as end-stage renal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588237.RA6ut48su7-RSqPWBbfICSBYfRUKZA29WhViqzPn0OC_g130_provenance.
- assertion description "[Lack of NPHP2 mutations in a newborn infant with Joubert syndrome-related disorder presenting as end-stage renal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP588241.RAHnefOuA8XEIY_liAV0JHFwaDsxe4jZpOX7ynV-gGzq0130_assertion description "[Lack of NPHP2 mutations in a newborn infant with Joubert syndrome-related disorder presenting as end-stage renal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588241.RAHnefOuA8XEIY_liAV0JHFwaDsxe4jZpOX7ynV-gGzq0130_provenance.
- NP886239.RArrwxiONdZx6Tez7bL4-ebzBZ7xnVjID7PsUwO6pGF-w130_assertion description "[Lack of NPHP2 mutations in a newborn infant with Joubert syndrome-related disorder presenting as end-stage renal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886239.RArrwxiONdZx6Tez7bL4-ebzBZ7xnVjID7PsUwO6pGF-w130_provenance.
- NP886261.RAlKoHFYJGvYfgFJU-2YHXBbUUpz2S9oMtIgywj7c5wt0130_assertion description "[Lack of NPHP2 mutations in a newborn infant with Joubert syndrome-related disorder presenting as end-stage renal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886261.RAlKoHFYJGvYfgFJU-2YHXBbUUpz2S9oMtIgywj7c5wt0130_provenance.