Matches in Nanopublications for { ?s ?p "[Large deletions in Xq21 often are associated with contiguous gene syndromes consisting of X-linked deafness type 3 (DFN3), mental retardation (MRX), and choroideremia (CHM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_assertion description "[Large deletions in Xq21 often are associated with contiguous gene syndromes consisting of X-linked deafness type 3 (DFN3), mental retardation (MRX), and choroideremia (CHM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_provenance.
- NP212382.RAyJ5y3Cre-yUoty0h7TdUVPQk-KcRZcrhc5DB2UyCvUk130_assertion description "[Large deletions in Xq21 often are associated with contiguous gene syndromes consisting of X-linked deafness type 3 (DFN3), mental retardation (MRX), and choroideremia (CHM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212382.RAyJ5y3Cre-yUoty0h7TdUVPQk-KcRZcrhc5DB2UyCvUk130_provenance.
- NP880741.RAb5IcPMO_D82IbEKn_qqoss4NyiCE_KWBMJWZOZ3cJt4130_assertion description "[Large deletions in Xq21 often are associated with contiguous gene syndromes consisting of X-linked deafness type 3 (DFN3), mental retardation (MRX), and choroideremia (CHM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP880741.RAb5IcPMO_D82IbEKn_qqoss4NyiCE_KWBMJWZOZ3cJt4130_provenance.
- NP635692.RAHGHF-X4789WVvS55cnrXccoS203Hcv0VSR2ieaUEUVA130_assertion description "[Large deletions in Xq21 often are associated with contiguous gene syndromes consisting of X-linked deafness type 3 (DFN3), mental retardation (MRX), and choroideremia (CHM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP635692.RAHGHF-X4789WVvS55cnrXccoS203Hcv0VSR2ieaUEUVA130_provenance.
- NP273065.RAH_BUTH1hkrM3iI-6nogLMNg-vdxGiNMHBCMDSx7IJ20130_assertion description "[Large deletions in Xq21 often are associated with contiguous gene syndromes consisting of X-linked deafness type 3 (DFN3), mental retardation (MRX), and choroideremia (CHM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP273065.RAH_BUTH1hkrM3iI-6nogLMNg-vdxGiNMHBCMDSx7IJ20130_provenance.