Detection of RET protooncogene mutation in the diagnosis of multiple endocrine neoplasia type 2 (MEN 2);Nachweis von RET-Proto-Onkogen-Mutationen zur Diagnostik der multiplen endokrinen Noeplasie Typ 2 (MEN 2)

Schweizerische Medizinische Wochenschrift

Volumn 126, Issue 31-32, 1996, Pages 1329-1338

  Komminoth, P ^a   Muletta Feurer, S ^a   Soltermann, A ^a   Gemsenjager, E ^a   Burgi, H ^a   Staub, J J ^a   Schonle, E ^a   Fried, M ^a   Vetter, W ^a   Spinas, G A ^a   Heitz, P U ^a  

^a UNIVERSITY OF ZURICH   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID SUBSTITUTION; ARTICLE; DNA DETERMINATION; DNA SEQUENCE; EXON; GEL ELECTROPHORESIS; GENE MUTATION; GERM LINE; HETEROZYGOTE; HUMAN; MALE; MULTIPLE ENDOCRINE NEOPLASIA; PHEOCHROMOCYTOMA; POINT MUTATION; POLYMERASE CHAIN REACTION; PROTO ONCOGENE; SEQUENCE ANALYSIS; SINGLE STRAND CONFORMATION POLYMORPHISM; THYROID MEDULLARY CARCINOMA; THYROIDECTOMY;

ADRENAL GLAND NEOPLASMS; AMINO ACID SEQUENCE; BASE SEQUENCE; CARCINOMA, MEDULLARY; DNA, NEOPLASM; DROSOPHILA PROTEINS; HETEROZYGOTE DETECTION; HUMANS; MOLECULAR SEQUENCE DATA; MULTIPLE ENDOCRINE NEOPLASIA TYPE 2A; PHEOCHROMOCYTOMA; POINT MUTATION; PROTO-ONCOGENE PROTEINS; PROTO-ONCOGENE PROTEINS C-RET; RECEPTOR PROTEIN-TYROSINE KINASES; THYROID NEOPLASMS;

EID: 0029974912     PISSN: 00367672     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)