Matches in Nanopublications for { ?s ?p "[Our results confirm that congenital Rett syndrome can be caused by copy-number variation in FOXG1 and expand the clinical phenotypic spectrum of FOXG1 defect in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP437623.RAY7S1m5hoSYtPnPsTOCngeIE5mEcF-r4_EXdd7AsKLlY130_assertion description "[Our results confirm that congenital Rett syndrome can be caused by copy-number variation in FOXG1 and expand the clinical phenotypic spectrum of FOXG1 defect in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP437623.RAY7S1m5hoSYtPnPsTOCngeIE5mEcF-r4_EXdd7AsKLlY130_provenance.
- assertion description "[Our results confirm that congenital Rett syndrome can be caused by copy-number variation in FOXG1 and expand the clinical phenotypic spectrum of FOXG1 defect in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP752800.RApdTuB6pN4oreaWJt0Js_SXcz-D325AJYcqZDJwzn6EY130_assertion description "[Our results confirm that congenital Rett syndrome can be caused by copy-number variation in FOXG1 and expand the clinical phenotypic spectrum of FOXG1 defect in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP752800.RApdTuB6pN4oreaWJt0Js_SXcz-D325AJYcqZDJwzn6EY130_provenance.