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

American Journal of Medical Genetics

Volumn 129 A, Issue 3, 2004, Pages 323-325

  Fitze, Guido ^a   Roesner, Dietmar ^a   Schreiber, Matthias ^b   Hohenberger, Werner ^b   Hümmer, Hans Peter ^b   Schackert, Hans K ^a  

^a DRESDEN UNIVERSITY OF TECHNOLOGY   (Germany)

^b UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN RET;

ALLELE; CODON; DNA EXTRACTION; DNA SEQUENCE; FAMILIAL CANCER; FAMILY STUDY; GENE AMPLIFICATION; GENE MUTATION; GENETIC POLYMORPHISM; HAPLOTYPE; HIRSCHSPRUNG DISEASE; HUMAN; LETTER; MISSENSE MUTATION; MUTATIONAL ANALYSIS; PENETRANCE; PHENOTYPE; PRIORITY JOURNAL; PROTO ONCOGENE; SIPPLE SYNDROME; THYROID MEDULLARY CARCINOMA;

CODON; GERM-LINE MUTATION; HAPLOTYPES; HIRSCHSPRUNG DISEASE; HUMANS; MULTIPLE ENDOCRINE NEOPLASIA TYPE 2A; ONCOGENE PROTEINS; PEDIGREE; PHENOTYPE; PROTO-ONCOGENE PROTEINS C-RET; RECEPTOR PROTEIN-TYROSINE KINASES; SEQUENCE ANALYSIS, DNA; THYROID GLAND;

EID: 4444247702     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30230     Document Type: Letter

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