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Items: 2

1.

Association between c135G/A genotype and RET proto-oncogene germline mutations and phenotype of Hirschsprung's disease.

Fitze G, Cramer J, Ziegler A, Schierz M, Schreiber M, Kuhlisch E, Roesner D, Schackert HK.

Lancet. 2002 Apr 6;359(9313):1200-5.

PMID:
11955539
2.

Interaction of RET proto-oncogene codon 609 germline mutations with RET haplotypes characterized by c.135G>A alleles modifying MEN 2A or HSCR phenotypes.

Fitze G, Schreiber M, Hohenberger W, Hümmer HP, Roesner D, Schackert HK.

Am J Med Genet A. 2004 Sep 1;129A(3):323-5. No abstract available.

PMID:
15326638

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