Matches in Nanopublications for { ?s ?p "[A translocation between Xq21.33 and 22q13.33 causes an intragenic SHANK3 deletion in a woman with Phelan-McDermid syndrome and hypergonadotropic hypogonadism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP841355.RA6QiNWm2HBhFWTeKW_ADJB_p4Id2FSJ71cphwH7DA1Bk130_assertion description "[A translocation between Xq21.33 and 22q13.33 causes an intragenic SHANK3 deletion in a woman with Phelan-McDermid syndrome and hypergonadotropic hypogonadism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP841355.RA6QiNWm2HBhFWTeKW_ADJB_p4Id2FSJ71cphwH7DA1Bk130_provenance.
- assertion description "[A translocation between Xq21.33 and 22q13.33 causes an intragenic SHANK3 deletion in a woman with Phelan-McDermid syndrome and hypergonadotropic hypogonadism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP868162.RAG_fXXaTpLns8IsrTWFBcXEjNzaRVsbZU9v4LDUdE9p0130_assertion description "[A translocation between Xq21.33 and 22q13.33 causes an intragenic SHANK3 deletion in a woman with Phelan-McDermid syndrome and hypergonadotropic hypogonadism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868162.RAG_fXXaTpLns8IsrTWFBcXEjNzaRVsbZU9v4LDUdE9p0130_provenance.