The role of ret genomic variants in infantile hypertrophic pyloric stenosis

European Journal of Pediatric Surgery

Volumn 21, Issue 6, 2011, Pages 389-394

  Serra, A ^a   Schuchardt, K ^b   Genuneit, J ^a   Leriche, C ^a   Grgens, H S ^b   Schackert, H K ^b   Fitze, G ^b  

^a UNIVERSITY OF ULM   (Germany)

^b DRESDEN UNIVERSITY OF TECHNOLOGY   (Germany)

Author keywords

infantile hypertrophic pyloric stenosis; mutations; polymorphisms; RET proto oncogene

Indexed keywords

PROTEIN RET;

ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; FAMILIAL INCIDENCE; FEMALE; GENE FREQUENCY; GENE LOCATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC CODE; GENETIC VARIABILITY; GENOME ANALYSIS; HUMAN; HUMAN CELL; HYPERTROPHIC PYLORUS STENOSIS; INFANT; INFANT DISEASE; INFANTILE HYPERTROPHIC PYLORUS STENOSIS; MALE; ONCOGENE RET; PROTO ONCOGENE;

ADULT; DNA; EXONS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; INFANT; INFANT, NEWBORN; MALE; MITOGENS; MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; PROTO-ONCOGENE PROTEINS C-RET; PYLORIC STENOSIS, HYPERTROPHIC;

EID: 84155163027     PISSN: 09397248     EISSN: 1439359X     Source Type: Journal    
DOI: 10.1055/s-0031-1291357     Document Type: Article

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