Matches in Nanopublications for { ?s ?p "[Taken together, our data suggest that rare deleterious CHD7 alleles contribute to the mutational burden of patients with both KS and normosmic forms of IGD in the absence of full CHARGE syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Taken together, our data suggest that rare deleterious CHD7 alleles contribute to the mutational burden of patients with both KS and normosmic forms of IGD in the absence of full CHARGE syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Taken together, our data suggest that rare deleterious CHD7 alleles contribute to the mutational burden of patients with both KS and normosmic forms of IGD in the absence of full CHARGE syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1244643.RAX8eJM_CQe_NJBKdn1F6Ig91aGKBUHv0tZileFHb-T44130_assertion description "[Taken together, our data suggest that rare deleterious CHD7 alleles contribute to the mutational burden of patients with both KS and normosmic forms of IGD in the absence of full CHARGE syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244643.RAX8eJM_CQe_NJBKdn1F6Ig91aGKBUHv0tZileFHb-T44130_provenance.
- NP1244644.RAbDngRMa5c7gBRwVD7hD5wqjdbPoPq2ynWUzJ0nC0HWU130_assertion description "[Taken together, our data suggest that rare deleterious CHD7 alleles contribute to the mutational burden of patients with both KS and normosmic forms of IGD in the absence of full CHARGE syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244644.RAbDngRMa5c7gBRwVD7hD5wqjdbPoPq2ynWUzJ0nC0HWU130_provenance.