Matches in Nanopublications for { ?s ?p "[We propose that these mutations are the molecular cause of the disease observed in the previously described SCKL2 family and in an additional unrelated family diagnosed with a similar form of congenital microcephaly termed Jawad syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP875073.RAcOUNFeEIMzB-OSWbv9PbYUVFX43gL161fd77tpcyiM4130_assertion description "[We propose that these mutations are the molecular cause of the disease observed in the previously described SCKL2 family and in an additional unrelated family diagnosed with a similar form of congenital microcephaly termed Jawad syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP875073.RAcOUNFeEIMzB-OSWbv9PbYUVFX43gL161fd77tpcyiM4130_provenance.
- NP404332.RA19gebTP-Mka0TX64TrpaJzQ81WkTVfICWx9jxOmHNlY130_assertion description "[We propose that these mutations are the molecular cause of the disease observed in the previously described SCKL2 family and in an additional unrelated family diagnosed with a similar form of congenital microcephaly termed Jawad syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404332.RA19gebTP-Mka0TX64TrpaJzQ81WkTVfICWx9jxOmHNlY130_provenance.
- NP667558.RASIeT_gQNkfBKSXSJvdRVvDAQb-iame-xe6z6BK45HYQ130_assertion description "[We propose that these mutations are the molecular cause of the disease observed in the previously described SCKL2 family and in an additional unrelated family diagnosed with a similar form of congenital microcephaly termed Jawad syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP667558.RASIeT_gQNkfBKSXSJvdRVvDAQb-iame-xe6z6BK45HYQ130_provenance.
- assertion description "[We propose that these mutations are the molecular cause of the disease observed in the previously described SCKL2 family and in an additional unrelated family diagnosed with a similar form of congenital microcephaly termed Jawad syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[We propose that these mutations are the molecular cause of the disease observed in the previously described SCKL2 family and in an additional unrelated family diagnosed with a similar form of congenital microcephaly termed Jawad syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP931084.RAsKmI3kmgz9oUtLf2DulmsiavGGgPEM5fTgZuzE-RCUo130_assertion description "[We propose that these mutations are the molecular cause of the disease observed in the previously described SCKL2 family and in an additional unrelated family diagnosed with a similar form of congenital microcephaly termed Jawad syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP931084.RAsKmI3kmgz9oUtLf2DulmsiavGGgPEM5fTgZuzE-RCUo130_provenance.
- NP667548.RALg4wEDlGyG0pf0I3EBk8ZE0J_MB1u2Qusst0hHqzXkw130_assertion description "[We propose that these mutations are the molecular cause of the disease observed in the previously described SCKL2 family and in an additional unrelated family diagnosed with a similar form of congenital microcephaly termed Jawad syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP667548.RALg4wEDlGyG0pf0I3EBk8ZE0J_MB1u2Qusst0hHqzXkw130_provenance.
- NP931085.RA0uz_n26BmQwH0eh2MbWbk66YUogTn19KfPTdrua1g2I130_assertion description "[We propose that these mutations are the molecular cause of the disease observed in the previously described SCKL2 family and in an additional unrelated family diagnosed with a similar form of congenital microcephaly termed Jawad syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP931085.RA0uz_n26BmQwH0eh2MbWbk66YUogTn19KfPTdrua1g2I130_provenance.