Matches in Nanopublications for { ?s ?p "[A novel MIP gene mutation associated with autosomal dominant congenital cataracts in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_assertion description "[A novel MIP gene mutation associated with autosomal dominant congenital cataracts in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_provenance.
- NP1143488.RACVymnxxBGgyXBCb6pVhxNZa56S_UO7sXoZDzlZ6XVcQ130_assertion description "[A novel MIP gene mutation associated with autosomal dominant congenital cataracts in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1143488.RACVymnxxBGgyXBCb6pVhxNZa56S_UO7sXoZDzlZ6XVcQ130_provenance.
- NP557016.RAT-vqC9JoeRbFPQJQYOrj7tZ4gODv0Y5SttIa-ZfBT7I130_assertion description "[A novel MIP gene mutation associated with autosomal dominant congenital cataracts in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557016.RAT-vqC9JoeRbFPQJQYOrj7tZ4gODv0Y5SttIa-ZfBT7I130_provenance.
- NP1009066.RAyMLdYI5U-vJ28CrBImCdi8m82n4i1uwjXygCHy_3QRU130_assertion description "[A novel MIP gene mutation associated with autosomal dominant congenital cataracts in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1009066.RAyMLdYI5U-vJ28CrBImCdi8m82n4i1uwjXygCHy_3QRU130_provenance.
- NP1143491.RA7wzBZV--Cqc2h8kJfHHTzkKJ00sCBGQbnXaV38BtjtU130_assertion description "[A novel MIP gene mutation associated with autosomal dominant congenital cataracts in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1143491.RA7wzBZV--Cqc2h8kJfHHTzkKJ00sCBGQbnXaV38BtjtU130_provenance.
- NP526951.RAHz92iaPMeKEXTkMoY5ockpDuuXAlFHwLo0iwsnzIXcc130_assertion description "[A novel MIP gene mutation associated with autosomal dominant congenital cataracts in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP526951.RAHz92iaPMeKEXTkMoY5ockpDuuXAlFHwLo0iwsnzIXcc130_provenance.
- NP1143489.RAqFfEZYiYQATr1Lm5cItwV_19Z1ycyg7e7wbgWZpMHhs130_assertion description "[A novel MIP gene mutation associated with autosomal dominant congenital cataracts in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1143489.RAqFfEZYiYQATr1Lm5cItwV_19Z1ycyg7e7wbgWZpMHhs130_provenance.
- NP1143490.RAhcVwh967erdAbuvQ_JBJvpy-NXkG2USwh2xX5CAivVI130_assertion description "[A novel MIP gene mutation associated with autosomal dominant congenital cataracts in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1143490.RAhcVwh967erdAbuvQ_JBJvpy-NXkG2USwh2xX5CAivVI130_provenance.