Matches in Nanopublications for { ?s ?p "[Our findings demonstrate a novel genomic disorder characterised by deletion of BMP2 with variable cognitive deficits and dysmorphic features and show that individuals bearing microdeletions in 20p12.3 often present with WPW syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP857214.RAAc8xQxOsKfAKz3DaQv72tVp9BykQriiYUfYcBIbMkPE130_assertion description "[Our findings demonstrate a novel genomic disorder characterised by deletion of BMP2 with variable cognitive deficits and dysmorphic features and show that individuals bearing microdeletions in 20p12.3 often present with WPW syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP857214.RAAc8xQxOsKfAKz3DaQv72tVp9BykQriiYUfYcBIbMkPE130_provenance.
- NP599532.RAQsV-sCvebH2i7qXDCADai5JOcNC5dUB8K4g3EfUeuis130_assertion description "[Our findings demonstrate a novel genomic disorder characterised by deletion of BMP2 with variable cognitive deficits and dysmorphic features and show that individuals bearing microdeletions in 20p12.3 often present with WPW syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP599532.RAQsV-sCvebH2i7qXDCADai5JOcNC5dUB8K4g3EfUeuis130_provenance.
- NP714422.RAC6mjOHkVP5LToJMcRNBG6FP0GQEbeJIJfwUK6d1-f3Y130_assertion description "[Our findings demonstrate a novel genomic disorder characterised by deletion of BMP2 with variable cognitive deficits and dysmorphic features and show that individuals bearing microdeletions in 20p12.3 often present with WPW syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP714422.RAC6mjOHkVP5LToJMcRNBG6FP0GQEbeJIJfwUK6d1-f3Y130_provenance.
- assertion description "[Our findings demonstrate a novel genomic disorder characterised by deletion of BMP2 with variable cognitive deficits and dysmorphic features and show that individuals bearing microdeletions in 20p12.3 often present with WPW syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Our findings demonstrate a novel genomic disorder characterised by deletion of BMP2 with variable cognitive deficits and dysmorphic features and show that individuals bearing microdeletions in 20p12.3 often present with WPW syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Our findings demonstrate a novel genomic disorder characterised by deletion of BMP2 with variable cognitive deficits and dysmorphic features and show that individuals bearing microdeletions in 20p12.3 often present with WPW syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Our findings demonstrate a novel genomic disorder characterised by deletion of BMP2 with variable cognitive deficits and dysmorphic features and show that individuals bearing microdeletions in 20p12.3 often present with WPW syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP269023.RAQFDWh6Rz0nRbVVDM5qghsl_6A-Ogk1AX-IisvCdaZCg130_assertion description "[Our findings demonstrate a novel genomic disorder characterised by deletion of BMP2 with variable cognitive deficits and dysmorphic features and show that individuals bearing microdeletions in 20p12.3 often present with WPW syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP269023.RAQFDWh6Rz0nRbVVDM5qghsl_6A-Ogk1AX-IisvCdaZCg130_provenance.
- NP269070.RAuvCwW9SoT_bx8IcvPv0_NHSIOX7sBodg47P70YJdpQk130_assertion description "[Our findings demonstrate a novel genomic disorder characterised by deletion of BMP2 with variable cognitive deficits and dysmorphic features and show that individuals bearing microdeletions in 20p12.3 often present with WPW syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP269070.RAuvCwW9SoT_bx8IcvPv0_NHSIOX7sBodg47P70YJdpQk130_provenance.
- NP269103.RAw_3AcbDyujM_JQK_VcHCWH26NQA-i5byK9VMc7QtxlA130_assertion description "[Our findings demonstrate a novel genomic disorder characterised by deletion of BMP2 with variable cognitive deficits and dysmorphic features and show that individuals bearing microdeletions in 20p12.3 often present with WPW syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP269103.RAw_3AcbDyujM_JQK_VcHCWH26NQA-i5byK9VMc7QtxlA130_provenance.
- NP694556.RAOGdus6lt3TO5jRDoPLW057i4Kk49ema4smIyyoQTFu8130_assertion description "[Our findings demonstrate a novel genomic disorder characterised by deletion of BMP2 with variable cognitive deficits and dysmorphic features and show that individuals bearing microdeletions in 20p12.3 often present with WPW syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694556.RAOGdus6lt3TO5jRDoPLW057i4Kk49ema4smIyyoQTFu8130_provenance.
- NP694557.RALmunBU5fRDIRf42NgERdmQYkDEE27D-mpj49kGuPgh8130_assertion description "[Our findings demonstrate a novel genomic disorder characterised by deletion of BMP2 with variable cognitive deficits and dysmorphic features and show that individuals bearing microdeletions in 20p12.3 often present with WPW syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694557.RALmunBU5fRDIRf42NgERdmQYkDEE27D-mpj49kGuPgh8130_provenance.