Matches in Nanopublications for { ?s ?p "[It seems that examination of sporadic or familial MM cases for the 1100delC germline mutation in CHK2 is not justified. To evaluate whether this CHK2 founder mutation is associated with MM in patients with LFS syndrome, more MM cases from LFS families should be examined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP59834.RAjIbFgX4xRKRtnk4KxWYPgXvoovGDA7AUkuR48L2oZKw130_assertion description "[It seems that examination of sporadic or familial MM cases for the 1100delC germline mutation in CHK2 is not justified. To evaluate whether this CHK2 founder mutation is associated with MM in patients with LFS syndrome, more MM cases from LFS families should be examined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59834.RAjIbFgX4xRKRtnk4KxWYPgXvoovGDA7AUkuR48L2oZKw130_provenance.