Matches in Nanopublications for { ?s ?p "[Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_assertion description "[Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_provenance.
- NP7879.RAaNxfLAocDO0Yuf2IQ7s7rdoGy46RZ2zx8Gd1iwWwnCs130_assertion description "[Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7879.RAaNxfLAocDO0Yuf2IQ7s7rdoGy46RZ2zx8Gd1iwWwnCs130_provenance.
- assertion description "[Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1176758.RAnEOXvrLB2fnRuxLXcMW1b3iwUDZGJe7SgmIsCc57qHE130_assertion description "[Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1176758.RAnEOXvrLB2fnRuxLXcMW1b3iwUDZGJe7SgmIsCc57qHE130_provenance.