Analysis of microdeletions in 22q11 in Colombian patients with congenital heart disease

Cardiac defects are the most frequent congenital malformations, with an incidence estimated between 4 and 12 per 1000 newborns. Their etiology is multifactorial and might be attributed to genetic predispositions and environmental factors. Since 1990 these types of pathologies have been associated wi...

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Autores:

Tipo de recurso:

Fecha de publicación:

2011

Institución:

Universidad del Rosario

Repositorio:

Repositorio EdocUR - U. Rosario

Idioma:

eng

OAI Identifier:

oai:repository.urosario.edu.co:10336/22190

Acceso en línea:

https://repository.urosario.edu.co/handle/10336/22190

Palabra clave:

Article
Chromosome deletion 22q11
Congenital heart disease
Fallot tetralogy
Genetic association
Heart atrium septum defect
Human
Major clinical study
Adolescent
Adult
Child
Chromosome deletion
Colombia
Dna mutational analysis
Female
Gene frequency
Genetic predisposition to disease
Humans
Infant
Male
Tetralogy of fallot
Young adult
Atrial septal defects
Congenital heart diseases
Densitometry
Microdeletion 22q11
Multiplex pcr
Tetralogy of fallot
Tuple 1
newborn
congenital
atrial
preschool
human
pair 22
Child
Chromosomes
Heart defects
Heart septal defects
Infant

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