Sentence and cancer type
Showing 501-520 of 577 items.
SentenceCancertype
Absence of mutations in the MEN2A region of the ret proto-oncogene in non-MEN 2A phaeochromocytomas. None
Exon structure and flanking intronic sequences of the human RET proto-oncogene. None
Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC. None
Identification of multiple endocrine neoplasia, type 2 gene carriers using linkage analysis and analysis of the RET proto-oncogene. None
Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours. None
Identification of the Cys634-->Tyr mutation of the RET proto-oncogene in a pedigree with multiple endocrine neoplasia type 2A and localized cutaneous lichen amyloidosis. None
Inherited cancers associated with the RET proto-oncogene. None
A de novo mutation of the RET proto-oncogene in a patient with MEN 2A. None
A novel polymorphism in the coding sequence of the human RET proto-oncogene. None
Germ line mutations of the ret proto-oncogene in Japanese patients with multiple endocrine neoplasia type 2A and type 2B. None
Clinical value of direct DNA analysis of the RET proto-oncogene in families with multiple endocrine neoplasia type 2A. None
Somatic and MEN 2A de novo mutations identified in the RET proto-oncogene by screening of sporadic MTC:s. None
A 7 bp deletion of the RET proto-oncogene in familial Hirschsprung s disease. None
De-novo mutations of the RET proto-oncogene in Hirschsprung s disease. None
[Mutations of RET proto-oncogene in Hirschsprung disease]. None
DNA polymorphisms and conditions for SSCP analysis of the 20 exons of the ret proto-oncogene. None
Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A. None
Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC. None
Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung s disease. None
Mutations of the RET proto-oncogene in Hirschsprung s disease. None