Matches in Nanopublications for { ?s ?p "[Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP2928.RAGfeAVf64-0UogEGuuBNz9AZr4b-r-uGIglFMi_ETryY130_assertion description "[Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2928.RAGfeAVf64-0UogEGuuBNz9AZr4b-r-uGIglFMi_ETryY130_provenance.
- NP14.RAfYl2YsxGjI5V5lZtfDwApcmmvTVrsvUZFF1mSmeOoew130_assertion description "[Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP14.RAfYl2YsxGjI5V5lZtfDwApcmmvTVrsvUZFF1mSmeOoew130_provenance.
- NP990460.RAZiOvaVYebBWREfkXp9eMer8UTdTV_P7QUKCQ4Fjync8130_assertion description "[Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP990460.RAZiOvaVYebBWREfkXp9eMer8UTdTV_P7QUKCQ4Fjync8130_provenance.
- assertion description "[Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP6109.RAKJT9_1BCGDH9tFpiYfY9qYR5Bq4GddDBjFxAq63goM8130_assertion description "[Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6109.RAKJT9_1BCGDH9tFpiYfY9qYR5Bq4GddDBjFxAq63goM8130_provenance.
- NP792235.RALASzSLnp6bYP2KVTUFtOPFekHkgxl_Pv8F9jmI2j5hI130_assertion description "[Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP792235.RALASzSLnp6bYP2KVTUFtOPFekHkgxl_Pv8F9jmI2j5hI130_provenance.