Mutation analysis of the RET receptor tyrosine kinase in hirschsprung disease

Human Molecular Genetics

Volumn 4, Issue 5, 1995, Pages 821-830

  Angrist, Misha ^a   Bolk, Stacey ^a   Thiel, Bonnie ^a   Puffenberger, Erik G ^a   Hofstra, Robert M ^b   Buys, Charles H C M ^b   Cass, Daniel T ^c   Chakravarti, Aravinda ^a  

^a UNIVERSITY HOSPITALS OF CLEVELAND   (United States)

^b UNIVERSITY OF GRONINGEN   (Netherlands)

^c WESTMEAD HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN TYROSINE KINASE;

ARTICLE; GENE; GENE FREQUENCY; GENE MUTATION; GENOTYPE; HIRSCHSPRUNG DISEASE; HUMAN; INTESTINE OBSTRUCTION; PATHOGENESIS; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; SIPPLE SYNDROME; THYROID MEDULLARY CARCINOMA;

BASE SEQUENCE; DNA; DNA MUTATIONAL ANALYSIS; EXONS; FEMALE; GENOTYPE; HIRSCHSPRUNG DISEASE; HUMAN; MALE; MOLECULAR SEQUENCE DATA; MULTIPLE ENDOCRINE NEOPLASIA TYPE 2A; MUTATION; PEDIGREE; PHENOTYPE; POLYMERASE CHAIN REACTION; POLYMORPHISM (GENETICS); PROTO-ONCOGENE PROTEINS; RECEPTOR PROTEIN-TYROSINE KINASES; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0029069528     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/4.5.821     Document Type: Article

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