Matches in Nanopublications for { ?s ?p "[Novel splicing, missense, and deletion mutations in seven adenosine deaminase-deficient patients with late/delayed onset of combined immunodeficiency disease. Contribution of genotype to phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP207.RARdWpib2ofoy5nbuD2Xv7g1Ovtt_vxYbtlLlwiJPzKEI130_assertion description "[Novel splicing, missense, and deletion mutations in seven adenosine deaminase-deficient patients with late/delayed onset of combined immunodeficiency disease. Contribution of genotype to phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207.RARdWpib2ofoy5nbuD2Xv7g1Ovtt_vxYbtlLlwiJPzKEI130_provenance.
- assertion description "[Novel splicing, missense, and deletion mutations in seven adenosine deaminase-deficient patients with late/delayed onset of combined immunodeficiency disease. Contribution of genotype to phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Novel splicing, missense, and deletion mutations in seven adenosine deaminase-deficient patients with late/delayed onset of combined immunodeficiency disease. Contribution of genotype to phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP857287.RA6QGu04GqkqWdw08Fc-0s1OHBO94ThY5NJ7Evql3nnEE130_assertion description "[Novel splicing, missense, and deletion mutations in seven adenosine deaminase-deficient patients with late/delayed onset of combined immunodeficiency disease. Contribution of genotype to phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP857287.RA6QGu04GqkqWdw08Fc-0s1OHBO94ThY5NJ7Evql3nnEE130_provenance.
- NP740.RA6BA60-6p69TI5TrcTpBvzUTgGT3qsEdLL6nhUTOMvXg130_assertion description "[Novel splicing, missense, and deletion mutations in seven adenosine deaminase-deficient patients with late/delayed onset of combined immunodeficiency disease. Contribution of genotype to phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP740.RA6BA60-6p69TI5TrcTpBvzUTgGT3qsEdLL6nhUTOMvXg130_provenance.
- NP222774.RAMCw3ST3NFY1qd0Ghe39lDRlDsyzudleLJrNO5Io2OFs130_assertion description "[Novel splicing, missense, and deletion mutations in seven adenosine deaminase-deficient patients with late/delayed onset of combined immunodeficiency disease. Contribution of genotype to phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222774.RAMCw3ST3NFY1qd0Ghe39lDRlDsyzudleLJrNO5Io2OFs130_provenance.
- NP1336184.RAIGjq3tlRKrGen1RXACy5hEBQ-vy6_-8ez3vkX720HtU130_assertion description "[Novel splicing, missense, and deletion mutations in seven adenosine deaminase-deficient patients with late/delayed onset of combined immunodeficiency disease. Contribution of genotype to phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1336184.RAIGjq3tlRKrGen1RXACy5hEBQ-vy6_-8ez3vkX720HtU130_provenance.
- NP8803.RA5KdDsUlkQfB6tCDH3QRVRWKzz3ZpecbSX6zCM2DFd7Y130_assertion description "[Novel splicing, missense, and deletion mutations in seven adenosine deaminase-deficient patients with late/delayed onset of combined immunodeficiency disease. Contribution of genotype to phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8803.RA5KdDsUlkQfB6tCDH3QRVRWKzz3ZpecbSX6zCM2DFd7Y130_provenance.