Matches in Nanopublications for { ?s ?p "[In this study, we investigate the prevalence and phenotype/genotype correlation of connexin (CX) gene family variants in a cohort of children with nonsyndromic hearing loss (HL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP822801.RAUbFH8Jtf6ecSFrnI7eJ2KVEJjpy-IiD_DUXERjJiDdc130_assertion description "[In this study, we investigate the prevalence and phenotype/genotype correlation of connexin (CX) gene family variants in a cohort of children with nonsyndromic hearing loss (HL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP822801.RAUbFH8Jtf6ecSFrnI7eJ2KVEJjpy-IiD_DUXERjJiDdc130_provenance.
- NP1012310.RAmmNUnHHojC13PUjJdCBftKMnD18WS2t1IVLTdozIlbs130_assertion description "[In this study, we investigate the prevalence and phenotype/genotype correlation of connexin (CX) gene family variants in a cohort of children with nonsyndromic hearing loss (HL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1012310.RAmmNUnHHojC13PUjJdCBftKMnD18WS2t1IVLTdozIlbs130_provenance.