Matches in Nanopublications for { ?s ?p "[Mutations in the human ARX gene show unusually heterogeneous clinical presentations, including syndromic and nonsyndromic mental retardation, myoclonic epilepsy with spasticity, and lissencephaly with abnormal genitalia, that are believed to arise from an impairment of the embryonic mechanisms building the anterior central nervous system structures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP327463.RAo4VNIVLT89y71vR2uRJ-BwF3lSNIgYFKo3nj1Cj5vx4130_assertion description "[Mutations in the human ARX gene show unusually heterogeneous clinical presentations, including syndromic and nonsyndromic mental retardation, myoclonic epilepsy with spasticity, and lissencephaly with abnormal genitalia, that are believed to arise from an impairment of the embryonic mechanisms building the anterior central nervous system structures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP327463.RAo4VNIVLT89y71vR2uRJ-BwF3lSNIgYFKo3nj1Cj5vx4130_provenance.
- NP748820.RAa8vMuZZNDTysZryWGD8mQBG5KdCdkl-rXkXsnRWbuiE130_assertion description "[Mutations in the human ARX gene show unusually heterogeneous clinical presentations, including syndromic and nonsyndromic mental retardation, myoclonic epilepsy with spasticity, and lissencephaly with abnormal genitalia, that are believed to arise from an impairment of the embryonic mechanisms building the anterior central nervous system structures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748820.RAa8vMuZZNDTysZryWGD8mQBG5KdCdkl-rXkXsnRWbuiE130_provenance.
- NP908568.RAyC6HagA0FyboByS9EONMPhURnIrrJkN11kZ-g5UjuN0130_assertion description "[Mutations in the human ARX gene show unusually heterogeneous clinical presentations, including syndromic and nonsyndromic mental retardation, myoclonic epilepsy with spasticity, and lissencephaly with abnormal genitalia, that are believed to arise from an impairment of the embryonic mechanisms building the anterior central nervous system structures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP908568.RAyC6HagA0FyboByS9EONMPhURnIrrJkN11kZ-g5UjuN0130_provenance.
- NP460598.RAc9kbxGFaHi5vfyp9Cv5xakcQJw4dmot7nut3dxkTwGc130_assertion description "[Mutations in the human ARX gene show unusually heterogeneous clinical presentations, including syndromic and nonsyndromic mental retardation, myoclonic epilepsy with spasticity, and lissencephaly with abnormal genitalia, that are believed to arise from an impairment of the embryonic mechanisms building the anterior central nervous system structures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP460598.RAc9kbxGFaHi5vfyp9Cv5xakcQJw4dmot7nut3dxkTwGc130_provenance.
- NP460601.RATgJ8IJqlWBKfEGru-D4_Tf7Vkl4KsTzsqysZX8Om288130_assertion description "[Mutations in the human ARX gene show unusually heterogeneous clinical presentations, including syndromic and nonsyndromic mental retardation, myoclonic epilepsy with spasticity, and lissencephaly with abnormal genitalia, that are believed to arise from an impairment of the embryonic mechanisms building the anterior central nervous system structures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP460601.RATgJ8IJqlWBKfEGru-D4_Tf7Vkl4KsTzsqysZX8Om288130_provenance.
- NP770790.RAGlAcToz6uJ3yimAZq5H8sBSBzGcjjkIKkr2WHEcAuBQ130_assertion description "[Mutations in the human ARX gene show unusually heterogeneous clinical presentations, including syndromic and nonsyndromic mental retardation, myoclonic epilepsy with spasticity, and lissencephaly with abnormal genitalia, that are believed to arise from an impairment of the embryonic mechanisms building the anterior central nervous system structures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP770790.RAGlAcToz6uJ3yimAZq5H8sBSBzGcjjkIKkr2WHEcAuBQ130_provenance.
- NP978150.RAoIcH4SrmUPi355nUqJf0vXIE4Wv3rQtxgNfgQuUvpRU130_assertion description "[Mutations in the human ARX gene show unusually heterogeneous clinical presentations, including syndromic and nonsyndromic mental retardation, myoclonic epilepsy with spasticity, and lissencephaly with abnormal genitalia, that are believed to arise from an impairment of the embryonic mechanisms building the anterior central nervous system structures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978150.RAoIcH4SrmUPi355nUqJf0vXIE4Wv3rQtxgNfgQuUvpRU130_provenance.
- NP460599.RArlZHtb7PPCwCUFNUOBLbftoHlWdcWdXOFpfVYVMQ5Ro130_assertion description "[Mutations in the human ARX gene show unusually heterogeneous clinical presentations, including syndromic and nonsyndromic mental retardation, myoclonic epilepsy with spasticity, and lissencephaly with abnormal genitalia, that are believed to arise from an impairment of the embryonic mechanisms building the anterior central nervous system structures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP460599.RArlZHtb7PPCwCUFNUOBLbftoHlWdcWdXOFpfVYVMQ5Ro130_provenance.
- NP835520.RA9i2Jij7sIDbHrv97N0gA3PdkUuLTjUhj5ovT7WXbRtE130_assertion description "[Mutations in the human ARX gene show unusually heterogeneous clinical presentations, including syndromic and nonsyndromic mental retardation, myoclonic epilepsy with spasticity, and lissencephaly with abnormal genitalia, that are believed to arise from an impairment of the embryonic mechanisms building the anterior central nervous system structures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835520.RA9i2Jij7sIDbHrv97N0gA3PdkUuLTjUhj5ovT7WXbRtE130_provenance.
- NP460600.RAJhUerzmitmRdNJGVFnefalSerSh0l3MbBh-zOiFJi5Y130_assertion description "[Mutations in the human ARX gene show unusually heterogeneous clinical presentations, including syndromic and nonsyndromic mental retardation, myoclonic epilepsy with spasticity, and lissencephaly with abnormal genitalia, that are believed to arise from an impairment of the embryonic mechanisms building the anterior central nervous system structures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP460600.RAJhUerzmitmRdNJGVFnefalSerSh0l3MbBh-zOiFJi5Y130_provenance.