Matches in Nanopublications for { ?s ?p "[The much rarer Jervell-Lange-Nielsen syndrome (with marked QT prolongation and sensorineural deafness) arises when a child inherits mutant KVLQT1 or minK alleles from both parents.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP338183.RAskwXDZbylDLT7Ix4s7O3Rp-wP6Kua5kHySKbgxLSuqQ130_assertion description "[The much rarer Jervell-Lange-Nielsen syndrome (with marked QT prolongation and sensorineural deafness) arises when a child inherits mutant KVLQT1 or minK alleles from both parents.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP338183.RAskwXDZbylDLT7Ix4s7O3Rp-wP6Kua5kHySKbgxLSuqQ130_provenance.
- NP289260.RAz5elVnLS2YuGWIvqcCnB16epHYbOxN7a3Rb0e-4XAlc130_assertion description "[The much rarer Jervell-Lange-Nielsen syndrome (with marked QT prolongation and sensorineural deafness) arises when a child inherits mutant KVLQT1 or minK alleles from both parents.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP289260.RAz5elVnLS2YuGWIvqcCnB16epHYbOxN7a3Rb0e-4XAlc130_provenance.
- assertion description "[The much rarer Jervell-Lange-Nielsen syndrome (with marked QT prolongation and sensorineural deafness) arises when a child inherits mutant KVLQT1 or minK alleles from both parents.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The much rarer Jervell-Lange-Nielsen syndrome (with marked QT prolongation and sensorineural deafness) arises when a child inherits mutant KVLQT1 or minK alleles from both parents.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP523139.RAqQUzLERpkC6hfjfHgICBUF4AR559G5mNDt8NyL5q64k130_assertion description "[The much rarer Jervell-Lange-Nielsen syndrome (with marked QT prolongation and sensorineural deafness) arises when a child inherits mutant KVLQT1 or minK alleles from both parents.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523139.RAqQUzLERpkC6hfjfHgICBUF4AR559G5mNDt8NyL5q64k130_provenance.
- NP289262.RAjzlTt-K3aptsYF_l2nt_3KoN_x8YG7irkJaOV-l7nKQ130_assertion description "[The much rarer Jervell-Lange-Nielsen syndrome (with marked QT prolongation and sensorineural deafness) arises when a child inherits mutant KVLQT1 or minK alleles from both parents.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP289262.RAjzlTt-K3aptsYF_l2nt_3KoN_x8YG7irkJaOV-l7nKQ130_provenance.