Matches in Nanopublications for { ?s ?p "[In male patient 3 carrying a 22q11.21 microduplication inherited from his unaffected father, WES identified a novel missense variant in the OPHN1 X-linked intellectual disability gene inherited from the unaffected mother as a possible additional cause for developmental delay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- NP600792.RAg55nnP8x1QC29k6x-vPYkIlDh-NhBWqhI9teWEKMzHM130_assertion description "[In male patient 3 carrying a 22q11.21 microduplication inherited from his unaffected father, WES identified a novel missense variant in the OPHN1 X-linked intellectual disability gene inherited from the unaffected mother as a possible additional cause for developmental delay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600792.RAg55nnP8x1QC29k6x-vPYkIlDh-NhBWqhI9teWEKMzHM130_provenance.
- assertion description "[In male patient 3 carrying a 22q11.21 microduplication inherited from his unaffected father, WES identified a novel missense variant in the OPHN1 X-linked intellectual disability gene inherited from the unaffected mother as a possible additional cause for developmental delay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[In male patient 3 carrying a 22q11.21 microduplication inherited from his unaffected father, WES identified a novel missense variant in the OPHN1 X-linked intellectual disability gene inherited from the unaffected mother as a possible additional cause for developmental delay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP603242.RAB0Mu6UcOGvBVkHyAVn5QOGO25eJLTb9jfBmBWRqaoDk130_assertion description "[In male patient 3 carrying a 22q11.21 microduplication inherited from his unaffected father, WES identified a novel missense variant in the OPHN1 X-linked intellectual disability gene inherited from the unaffected mother as a possible additional cause for developmental delay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP603242.RAB0Mu6UcOGvBVkHyAVn5QOGO25eJLTb9jfBmBWRqaoDk130_provenance.
- NP1066050.RAI54RPrMbxxpZjL17W7HoAPs9CcfOEpWmVLZaf5v1lM4130_assertion description "[In male patient 3 carrying a 22q11.21 microduplication inherited from his unaffected father, WES identified a novel missense variant in the OPHN1 X-linked intellectual disability gene inherited from the unaffected mother as a possible additional cause for developmental delay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1066050.RAI54RPrMbxxpZjL17W7HoAPs9CcfOEpWmVLZaf5v1lM4130_provenance.