Matches in Nanopublications for { ?s ?p "[Cohen syndrome is an autosomal recessive, multiple congenital anomalies/mental retardation (MCA/MR) syndrome, caused by a mutation in the COH1 gen, localized on chromosome 8q22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP447033.RAmBH0Xmoq9J1DAAd9qgVjndafyA-I45gmr6-J3RB6Cs0130_assertion description "[Cohen syndrome is an autosomal recessive, multiple congenital anomalies/mental retardation (MCA/MR) syndrome, caused by a mutation in the COH1 gen, localized on chromosome 8q22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP447033.RAmBH0Xmoq9J1DAAd9qgVjndafyA-I45gmr6-J3RB6Cs0130_provenance.
- NP802318.RAzJSrbb2G9S2SJOY8DhyX3GCq2SVUuw-vS0tSA_Fl5aA130_assertion description "[Cohen syndrome is an autosomal recessive, multiple congenital anomalies/mental retardation (MCA/MR) syndrome, caused by a mutation in the COH1 gen, localized on chromosome 8q22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802318.RAzJSrbb2G9S2SJOY8DhyX3GCq2SVUuw-vS0tSA_Fl5aA130_provenance.