Familial associations in medullary thyroid carcinoma with Hirschsprung disease: the role of the RET-C620 “Janus” genetic variation
Author:
Publisher
Elsevier BV
Subject
General Medicine,Pediatrics, Perinatology, and Child Health,Surgery
Reference29 articles.
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2. A novel Czech kindred with familial medullary thyroid carcinoma and Hirschsprung's disease;Dvorakova;J Pediatr Surg,2005
3. Diverse phenotypes associated with exon 10 mutations of the RET proto-oncogene;Mulligan;Hum Mol Genet,1994
4. C618R mutation in exon 10 of the RET proto-oncogene in a kindred with multiple endocrine neoplasia type 2A and Hirschsprung's disease;Caron;J Clin Endocrinol Metab,1996
5. Cys 618 Arg mutation in the RET proto-oncogene associated with familial medullary thyroid carcinoma and maternally transmitted Hirschsprung's disease suggesting a role for imprinting;PeRETz;Hum Mutat,1997
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4. Comprehensive characterization of the genetic landscape of familial Hirschsprung’s disease;World Journal of Pediatrics;2023-03-01
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