Matches in Nanopublications for { ?s ?p "[Analysis of the CRELD1 gene from individuals with non-trisomy 21-associated AVSD identified heterozygous missense mutations in nearly 6% of this population, including mutations in isolated AVSD and AVSD associated with heterotaxy syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP182744.RAaLaNoxhZ-lV0PWOkdus157C5LSc_zH8yXEIMgt76MNY130_assertion description "[Analysis of the CRELD1 gene from individuals with non-trisomy 21-associated AVSD identified heterozygous missense mutations in nearly 6% of this population, including mutations in isolated AVSD and AVSD associated with heterotaxy syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182744.RAaLaNoxhZ-lV0PWOkdus157C5LSc_zH8yXEIMgt76MNY130_provenance.
- NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_assertion description "[Analysis of the CRELD1 gene from individuals with non-trisomy 21-associated AVSD identified heterozygous missense mutations in nearly 6% of this population, including mutations in isolated AVSD and AVSD associated with heterotaxy syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_provenance.
- NP941679.RAVxBDqFYIgAhXInS7aiMrUtAS9zg7gtX8sB9G95NgFPg130_assertion description "[Analysis of the CRELD1 gene from individuals with non-trisomy 21-associated AVSD identified heterozygous missense mutations in nearly 6% of this population, including mutations in isolated AVSD and AVSD associated with heterotaxy syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP941679.RAVxBDqFYIgAhXInS7aiMrUtAS9zg7gtX8sB9G95NgFPg130_provenance.
- assertion description "[Analysis of the CRELD1 gene from individuals with non-trisomy 21-associated AVSD identified heterozygous missense mutations in nearly 6% of this population, including mutations in isolated AVSD and AVSD associated with heterotaxy syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Analysis of the CRELD1 gene from individuals with non-trisomy 21-associated AVSD identified heterozygous missense mutations in nearly 6% of this population, including mutations in isolated AVSD and AVSD associated with heterotaxy syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP941702.RAAuMr2CDYvHRN5zaisz8q0bKwkl2uQdFFPItB5QgA-UU130_assertion description "[Analysis of the CRELD1 gene from individuals with non-trisomy 21-associated AVSD identified heterozygous missense mutations in nearly 6% of this population, including mutations in isolated AVSD and AVSD associated with heterotaxy syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP941702.RAAuMr2CDYvHRN5zaisz8q0bKwkl2uQdFFPItB5QgA-UU130_provenance.
- NP386783.RACPyaO5TsUvxpbECCE-X2FENE9C4OZTye3H7S78rZk1Q130_assertion description "[Analysis of the CRELD1 gene from individuals with non-trisomy 21-associated AVSD identified heterozygous missense mutations in nearly 6% of this population, including mutations in isolated AVSD and AVSD associated with heterotaxy syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP386783.RACPyaO5TsUvxpbECCE-X2FENE9C4OZTye3H7S78rZk1Q130_provenance.
- NP386785.RANYusrd7Zzxb5RqaL_GSf5ySfPIVWp0UBw6hz0O0v9IU130_assertion description "[Analysis of the CRELD1 gene from individuals with non-trisomy 21-associated AVSD identified heterozygous missense mutations in nearly 6% of this population, including mutations in isolated AVSD and AVSD associated with heterotaxy syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP386785.RANYusrd7Zzxb5RqaL_GSf5ySfPIVWp0UBw6hz0O0v9IU130_provenance.