Matches in Nanopublications for { ?s ?p "[Heterozygous missense mutations in PITX3 have been reported in patients with autosomal dominant congenital cataract and anterior segment (ocular) mesenchymal dysgenesis (ASMD) whereas homozygous missense mutations have been found in patients with microphthalmia and neurological impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP574754.RAf_Nz28yWoG6lujNCEEbMynBo11ixhk6WClU3_HTMbDA130_assertion description "[Heterozygous missense mutations in PITX3 have been reported in patients with autosomal dominant congenital cataract and anterior segment (ocular) mesenchymal dysgenesis (ASMD) whereas homozygous missense mutations have been found in patients with microphthalmia and neurological impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP574754.RAf_Nz28yWoG6lujNCEEbMynBo11ixhk6WClU3_HTMbDA130_provenance.
- NP163865.RAlg-RhKQ1Bje2d5Y5CiTqQdfab1_neDnLXpfPVz65XxQ130_assertion description "[Heterozygous missense mutations in PITX3 have been reported in patients with autosomal dominant congenital cataract and anterior segment (ocular) mesenchymal dysgenesis (ASMD) whereas homozygous missense mutations have been found in patients with microphthalmia and neurological impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163865.RAlg-RhKQ1Bje2d5Y5CiTqQdfab1_neDnLXpfPVz65XxQ130_provenance.
- NP501091.RAsWBT4ofblVkYMJI5sTCd2Ns9nBndP0W8YfGhRZU6PvI130_assertion description "[Heterozygous missense mutations in PITX3 have been reported in patients with autosomal dominant congenital cataract and anterior segment (ocular) mesenchymal dysgenesis (ASMD) whereas homozygous missense mutations have been found in patients with microphthalmia and neurological impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP501091.RAsWBT4ofblVkYMJI5sTCd2Ns9nBndP0W8YfGhRZU6PvI130_provenance.
- NP626537.RAXn-eWPmOOcGKtYDoFWAG-CQLYiX-JqKTs09p9agrjJo130_assertion description "[Heterozygous missense mutations in PITX3 have been reported in patients with autosomal dominant congenital cataract and anterior segment (ocular) mesenchymal dysgenesis (ASMD) whereas homozygous missense mutations have been found in patients with microphthalmia and neurological impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP626537.RAXn-eWPmOOcGKtYDoFWAG-CQLYiX-JqKTs09p9agrjJo130_provenance.
- NP837201.RAykjY62-IzxeS48OOh_qU7mBJ-WX9mv3Fvq6d0eN7Eew130_assertion description "[Heterozygous missense mutations in PITX3 have been reported in patients with autosomal dominant congenital cataract and anterior segment (ocular) mesenchymal dysgenesis (ASMD) whereas homozygous missense mutations have been found in patients with microphthalmia and neurological impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP837201.RAykjY62-IzxeS48OOh_qU7mBJ-WX9mv3Fvq6d0eN7Eew130_provenance.
- assertion description "[Heterozygous missense mutations in PITX3 have been reported in patients with autosomal dominant congenital cataract and anterior segment (ocular) mesenchymal dysgenesis (ASMD) whereas homozygous missense mutations have been found in patients with microphthalmia and neurological impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Heterozygous missense mutations in PITX3 have been reported in patients with autosomal dominant congenital cataract and anterior segment (ocular) mesenchymal dysgenesis (ASMD) whereas homozygous missense mutations have been found in patients with microphthalmia and neurological impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Heterozygous missense mutations in PITX3 have been reported in patients with autosomal dominant congenital cataract and anterior segment (ocular) mesenchymal dysgenesis (ASMD) whereas homozygous missense mutations have been found in patients with microphthalmia and neurological impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Heterozygous missense mutations in PITX3 have been reported in patients with autosomal dominant congenital cataract and anterior segment (ocular) mesenchymal dysgenesis (ASMD) whereas homozygous missense mutations have been found in patients with microphthalmia and neurological impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP626557.RADmBn5zSWIjzHZOo0ufIBTGIod9wpG1giLa9aSY9G0V4130_assertion description "[Heterozygous missense mutations in PITX3 have been reported in patients with autosomal dominant congenital cataract and anterior segment (ocular) mesenchymal dysgenesis (ASMD) whereas homozygous missense mutations have been found in patients with microphthalmia and neurological impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP626557.RADmBn5zSWIjzHZOo0ufIBTGIod9wpG1giLa9aSY9G0V4130_provenance.
- NP626568.RArRubLiKTCtEMOcB2JEx-l4ZJnFyzV0l9cPe_zSpoxtk130_assertion description "[Heterozygous missense mutations in PITX3 have been reported in patients with autosomal dominant congenital cataract and anterior segment (ocular) mesenchymal dysgenesis (ASMD) whereas homozygous missense mutations have been found in patients with microphthalmia and neurological impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP626568.RArRubLiKTCtEMOcB2JEx-l4ZJnFyzV0l9cPe_zSpoxtk130_provenance.
- NP951243.RAtVTvu8ZUpyjm49Jl8ein1IT29WFbJf4wkaaJmqULK78130_assertion description "[Heterozygous missense mutations in PITX3 have been reported in patients with autosomal dominant congenital cataract and anterior segment (ocular) mesenchymal dysgenesis (ASMD) whereas homozygous missense mutations have been found in patients with microphthalmia and neurological impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP951243.RAtVTvu8ZUpyjm49Jl8ein1IT29WFbJf4wkaaJmqULK78130_provenance.
- NP951245.RAk2NB8seCSNSrVcS0SQtYuSm0HaBKOJKDw8ge1-Uf7fI130_assertion description "[Heterozygous missense mutations in PITX3 have been reported in patients with autosomal dominant congenital cataract and anterior segment (ocular) mesenchymal dysgenesis (ASMD) whereas homozygous missense mutations have been found in patients with microphthalmia and neurological impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP951245.RAk2NB8seCSNSrVcS0SQtYuSm0HaBKOJKDw8ge1-Uf7fI130_provenance.
- NP951244.RA0veQ1W2L5auUb3qhbxsNCTpKxCSSVtzYpLYG5Xwc-jQ130_assertion description "[Heterozygous missense mutations in PITX3 have been reported in patients with autosomal dominant congenital cataract and anterior segment (ocular) mesenchymal dysgenesis (ASMD) whereas homozygous missense mutations have been found in patients with microphthalmia and neurological impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP951244.RA0veQ1W2L5auUb3qhbxsNCTpKxCSSVtzYpLYG5Xwc-jQ130_provenance.