Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP350.RAUTMmka1YPfZ_RaCB_UmDz3WEI4k5PfyaAj_6yPt4TPw130_assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP350.RAUTMmka1YPfZ_RaCB_UmDz3WEI4k5PfyaAj_6yPt4TPw130_provenance.
• NP79500.RAy8D2pIr8N4FcjK6ZYizMq0OM0FPbVJvmfZYw1zEhpvY130_assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79500.RAy8D2pIr8N4FcjK6ZYizMq0OM0FPbVJvmfZYw1zEhpvY130_provenance.
• assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP74418.RA7P5B4Rr8mNlgLsnifq9Jrp8WUYPKm5_YPjcpzjt72lI130_assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP74418.RA7P5B4Rr8mNlgLsnifq9Jrp8WUYPKm5_YPjcpzjt72lI130_provenance.
• NP352.RAIWuGP7gaJPCuA6eLVytqaaNz37E3FfFtR3bSLsr5Hwc130_assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP352.RAIWuGP7gaJPCuA6eLVytqaaNz37E3FfFtR3bSLsr5Hwc130_provenance.
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• NP236452.RAc60kEquN82b4ZwFNTyu_v7suBKU8ct37y0cC7iHzisg130_assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP236452.RAc60kEquN82b4ZwFNTyu_v7suBKU8ct37y0cC7iHzisg130_provenance.
• NP429776.RA2PMSMyLFZduDaqmWRo7Q-eKKCjXhE5pTPnk0HWWRTOU130_assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP429776.RA2PMSMyLFZduDaqmWRo7Q-eKKCjXhE5pTPnk0HWWRTOU130_provenance.
• NP4595.RAQ67bFspmCjaHnNi3zJuC7OnklA3j5LltuWHXygcEObo130_assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4595.RAQ67bFspmCjaHnNi3zJuC7OnklA3j5LltuWHXygcEObo130_provenance.
• NP415.RAgtLjWM2ytu3bavLV4TrkkKeZJT_zMxOGD1CdaOYBVaU130_assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP415.RAgtLjWM2ytu3bavLV4TrkkKeZJT_zMxOGD1CdaOYBVaU130_provenance.
• NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_provenance.
• NP935233.RAfFhZ8CiNY-xqD-cJ7mM9mus8VBsRpLJXPImYIchQ-4s130_assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP935233.RAfFhZ8CiNY-xqD-cJ7mM9mus8VBsRpLJXPImYIchQ-4s130_provenance.
• NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_provenance.
• NP118784.RABFnnaWX1Nzm8l_r1GLivBeIVQv27eo6UTwc7U4c4VUk130_assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP118784.RABFnnaWX1Nzm8l_r1GLivBeIVQv27eo6UTwc7U4c4VUk130_provenance.
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• assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP5646.RAp-MJoTZbMftj2i-V3FXg388_vmMPU3UYuLVM5XtTUQQ130_assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5646.RAp-MJoTZbMftj2i-V3FXg388_vmMPU3UYuLVM5XtTUQQ130_provenance.
• NP713082.RAqY_ZKuWV9rTjEzJpmsXWqZsiAgZyLVDPHdrU-SwHu0U130_assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP713082.RAqY_ZKuWV9rTjEzJpmsXWqZsiAgZyLVDPHdrU-SwHu0U130_provenance.
• NP106232.RA9isj_Bj6cFHx6TNQSIlrGvA68pRUSBm-G2KzZmsYszM130_assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP106232.RA9isj_Bj6cFHx6TNQSIlrGvA68pRUSBm-G2KzZmsYszM130_provenance.
• NP236446.RA1PSosgCxlLB-4u2f6JETGgmtZ3RITMNDMJhmHuWIz2w130_assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP236446.RA1PSosgCxlLB-4u2f6JETGgmtZ3RITMNDMJhmHuWIz2w130_provenance.
• NP137881.RAPE0xw4pTVCqVD03ccSbYXeob_vmEsE-CXGhKYVWndlQ130_assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP137881.RAPE0xw4pTVCqVD03ccSbYXeob_vmEsE-CXGhKYVWndlQ130_provenance.
• NP5645.RAxuBPWBASwgIZCoaZwgPouyH7VpLpmfT67ckU1agfHTE130_assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5645.RAxuBPWBASwgIZCoaZwgPouyH7VpLpmfT67ckU1agfHTE130_provenance.
• NP713083.RAI3o7RzNIgJvZNH4PiNTKfGNrAVRfWkM5ZqxO07HZKxc130_assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP713083.RAI3o7RzNIgJvZNH4PiNTKfGNrAVRfWkM5ZqxO07HZKxc130_provenance.
• NP713084.RA2x6zS8Df5kp7dGX5lOsBpR-_dS6-jSNXBOjT_RLt7fw130_assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP713084.RA2x6zS8Df5kp7dGX5lOsBpR-_dS6-jSNXBOjT_RLt7fw130_provenance.