Matches in Nanopublications for { ?s ?p "[A novel 3-base pair deletion of the CRYAA gene identified in a large Chinese pedigree featuring autosomal dominant congenital perinuclear cataract.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1267360.RABcVP_4Jk2DDq6BGQZe-b3RpeaLEjlAjcdcJboWSiB0c130_assertion description "[A novel 3-base pair deletion of the CRYAA gene identified in a large Chinese pedigree featuring autosomal dominant congenital perinuclear cataract.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1267360.RABcVP_4Jk2DDq6BGQZe-b3RpeaLEjlAjcdcJboWSiB0c130_provenance.
- NP1267361.RAF5ppJKV0HYYOwaJDQLNj5K-QD2DPnqc61-tLg69UUWw130_assertion description "[A novel 3-base pair deletion of the CRYAA gene identified in a large Chinese pedigree featuring autosomal dominant congenital perinuclear cataract.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1267361.RAF5ppJKV0HYYOwaJDQLNj5K-QD2DPnqc61-tLg69UUWw130_provenance.