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Matches in Nanopublications for { ?s ?p "[Comparison of the phenotypic features in a total of 19 patients with del(17)(p11.2p11.2) shows a consistent clinical phenotype with moderate to severe mental retardation, microbrachycelphaly, prominent forehead, broad face, flat midface, prognathism, short, broad hands, and behavioural anomalies such as self-mutilation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP313072.RAic91E2o8AIeZ4GawcNFO4z-OWqVHVMgWUsVIOuMpEvA130_assertion description "[Comparison of the phenotypic features in a total of 19 patients with del(17)(p11.2p11.2) shows a consistent clinical phenotype with moderate to severe mental retardation, microbrachycelphaly, prominent forehead, broad face, flat midface, prognathism, short, broad hands, and behavioural anomalies such as self-mutilation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP313072.RAic91E2o8AIeZ4GawcNFO4z-OWqVHVMgWUsVIOuMpEvA130_provenance.
• NP503972.RAvetO4peS37KkE8UkkvvJXlo1E6VnvBHE_9IFr7EPn5k130_assertion description "[Comparison of the phenotypic features in a total of 19 patients with del(17)(p11.2p11.2) shows a consistent clinical phenotype with moderate to severe mental retardation, microbrachycelphaly, prominent forehead, broad face, flat midface, prognathism, short, broad hands, and behavioural anomalies such as self-mutilation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP503972.RAvetO4peS37KkE8UkkvvJXlo1E6VnvBHE_9IFr7EPn5k130_provenance.
• NP521251.RAlgjwwX3msifcjkNRg1KfbIWx72LmCIzglTrzznufPAQ130_assertion description "[Comparison of the phenotypic features in a total of 19 patients with del(17)(p11.2p11.2) shows a consistent clinical phenotype with moderate to severe mental retardation, microbrachycelphaly, prominent forehead, broad face, flat midface, prognathism, short, broad hands, and behavioural anomalies such as self-mutilation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP521251.RAlgjwwX3msifcjkNRg1KfbIWx72LmCIzglTrzznufPAQ130_provenance.
• NP410347.RAQ7mmAm3m3-5P3HYuWsUI2GvUq95eBP2hj5ZLM28oLGA130_assertion description "[Comparison of the phenotypic features in a total of 19 patients with del(17)(p11.2p11.2) shows a consistent clinical phenotype with moderate to severe mental retardation, microbrachycelphaly, prominent forehead, broad face, flat midface, prognathism, short, broad hands, and behavioural anomalies such as self-mutilation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP410347.RAQ7mmAm3m3-5P3HYuWsUI2GvUq95eBP2hj5ZLM28oLGA130_provenance.
• NP769939.RACk5-7Qj9Ki08NohvB9qPlS2ube8OmjRaMWlHQZdbgDc130_assertion description "[Comparison of the phenotypic features in a total of 19 patients with del(17)(p11.2p11.2) shows a consistent clinical phenotype with moderate to severe mental retardation, microbrachycelphaly, prominent forehead, broad face, flat midface, prognathism, short, broad hands, and behavioural anomalies such as self-mutilation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP769939.RACk5-7Qj9Ki08NohvB9qPlS2ube8OmjRaMWlHQZdbgDc130_provenance.
• NP650645.RAjgQbBwTzp9uMOEbagb1Z99uFJer8dZVLd5SR5cB68R8130_assertion description "[Comparison of the phenotypic features in a total of 19 patients with del(17)(p11.2p11.2) shows a consistent clinical phenotype with moderate to severe mental retardation, microbrachycelphaly, prominent forehead, broad face, flat midface, prognathism, short, broad hands, and behavioural anomalies such as self-mutilation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650645.RAjgQbBwTzp9uMOEbagb1Z99uFJer8dZVLd5SR5cB68R8130_provenance.
• NP811517.RAkYoOISImQ6-34NloyV34yXWojywLnHOpYd-l7-5odxc130_assertion description "[Comparison of the phenotypic features in a total of 19 patients with del(17)(p11.2p11.2) shows a consistent clinical phenotype with moderate to severe mental retardation, microbrachycelphaly, prominent forehead, broad face, flat midface, prognathism, short, broad hands, and behavioural anomalies such as self-mutilation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP811517.RAkYoOISImQ6-34NloyV34yXWojywLnHOpYd-l7-5odxc130_provenance.
• NP603186.RAdzyseTMwb9zfLPBuoWz5MwjPMb_8rlGi_MRu9d_Ci9Y130_assertion description "[Comparison of the phenotypic features in a total of 19 patients with del(17)(p11.2p11.2) shows a consistent clinical phenotype with moderate to severe mental retardation, microbrachycelphaly, prominent forehead, broad face, flat midface, prognathism, short, broad hands, and behavioural anomalies such as self-mutilation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP603186.RAdzyseTMwb9zfLPBuoWz5MwjPMb_8rlGi_MRu9d_Ci9Y130_provenance.
• NP849060.RAM8J748sqPLVBsCmCuduNQnrDJqCeBV8iw5CUZ8cNoVc130_assertion description "[Comparison of the phenotypic features in a total of 19 patients with del(17)(p11.2p11.2) shows a consistent clinical phenotype with moderate to severe mental retardation, microbrachycelphaly, prominent forehead, broad face, flat midface, prognathism, short, broad hands, and behavioural anomalies such as self-mutilation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP849060.RAM8J748sqPLVBsCmCuduNQnrDJqCeBV8iw5CUZ8cNoVc130_provenance.