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1 eral related neoplastic disorders, including Cowden disease.
2 irm the role of this gene in the etiology of Cowden disease.
3 ient with a clinical history consistent with Cowden disease.
4 in the germ line of patients with hereditary Cowden disease.
6 also identified as the gene predisposing to Cowden disease, an autosomal dominant cancer predisposit
7 a region harboring the gene responsible for Cowden disease, an autosomal dominant hamartoma syndrome
9 utations in PTEN have also been described in Cowden disease and in a small number of patients with ju
11 hereditary cancer predisposition syndromes, Cowden disease, and Bannayan-Zonana syndrome, wherein br
14 m-line mutations in PTEN are responsible for Cowden disease (CD), a rare autosomal dominant multiple-
16 related human autosomal dominant disorders, Cowden disease (CD), Lhermitte-Duclos disease (LDD) and
18 eptibility gene for two hamartoma syndromes: Cowden disease (CD; MIM 158350) and Bannayan-Zonana (BZS
20 n PTEN, PTEN-G129E, which is observed in two Cowden disease kindreds, specifically ablates the abilit
21 en described as different disorders, such as Cowden disease, Lhermitte-Duclos disease, and Bannayan-Z
22 lcaba syndrome, juvenile polyposis coli, and Cowden disease, may share the same genetic defect becaus
23 ion for the chemoprevention and treatment of Cowden disease patients and others tumor syndromes that
26 l dominant familial cancer syndrome known as Cowden disease, which includes breast cancer among its c
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