id	author	title	date	pages	extension	mime	words	sentences	flesch	summary	cache	txt
work_7vczsljwendo7oj6uhgeoyyiom	Guido Fitze	Association of RET Protooncogene Codon 45 Polymorphism with Hirschsprung Disease	1999	5	.pdf	application/pdf	4115	399	63	HSCR, 10%–40% have been reported to harbor germline mutations of the RET protooncogene, which are by Ceccherini et al., the allele frequencies of these polymorphisms were evaluated in a normal control group. Allele Frequencies of Polymorphic Variants of RET in 62 Patients with Sporadic HSCR and The population that we studied comprised 62 individuals with sporadic HSCR who were from two different Our data revealed that allele frequencies of all polymorphisms in the control population were similar to In addition, we found the codon 769 polymorphism to be associated with HSCR in both populations, Eng C, Mulligan LM (1997) Mutation of the RET protooncogene in the multiple endocrine neoplasia type 2 syndromes, related sporadic tumours, and Hirschsprung disease. In these families, we have observed a male-to-female ratio among the affected individuals that is strikingly different from the generally accepted ratio in the overall adult stuttering population. Association of RET Protooncogene Codon 45 Polymorphism with Hirschsprung Disease	./cache/work_7vczsljwendo7oj6uhgeoyyiom.pdf	./txt/work_7vczsljwendo7oj6uhgeoyyiom.txt