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Items: 6

1.

RET proto-oncogene mutations in French MEN 2A and FMTC families.

Schuffenecker I, Billaud M, Calender A, Chambe B, Ginet N, Calmettes C, Modigliani E, Lenoir GM.

Hum Mol Genet. 1994 Nov;3(11):1939-43.

PMID:
7874109
2.

Association of multiple endocrine neoplasia type 2 and Hirschsprung disease.

Romeo G, Ceccherini I, Celli J, Priolo M, Betsos N, Bonardi G, Seri M, Yin L, Lerone M, Jasonni V, Martucciello G.

J Intern Med. 1998 Jun;243(6):515-20.

3.

Molecular analysis of the ret and GDNF genes in a family with multiple endocrine neoplasia type 2A and Hirschsprung disease.

Borrego S, Eng C, Sánchez B, Sáez ME, Navarro E, Antiñolo G.

J Clin Endocrinol Metab. 1998 Sep;83(9):3361-4.

PMID:
9745455
4.

Mutational analysis of the RET proto-oncogene in a kindred with multiple endocrine neoplasia type 2A and Hirschsprung's disease.

Inoue K, Shimotake T, Inoue K, Tokiwa K, Iwai N.

J Pediatr Surg. 1999 Oct;34(10):1552-4.

PMID:
10549772
5.

Familial prevalence and age of RET germline mutations: implications for screening.

Machens A, Dralle H.

Clin Endocrinol (Oxf). 2008 Jul;69(1):81-7. Epub 2008 Jul 1.

PMID:
18062802
6.

The RET C620S mutation causes multiple endocrine neoplasia type 2A (MEN2A) but not Hirschsprung disease (HSCR) in a family cosegregating both phenotypes.

Fernández RM, Antiñolo G, Eng C, Borrego S.

Hum Mutat. 2003 Nov;22(5):412-5. No abstract available.

PMID:
14517954

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