Characterization of a t(5;8)(q31;q21) translocation in a patient with mental retardation and congenital heart disease: implications for involvement of RUNX1T1 in human brain and heart development.
Eur J Hum Genet
; 17(8): 1010-8, 2009 Aug.
Article
in En
| MEDLINE
| ID: mdl-19172993
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Transcription Factors
/
Translocation, Genetic
/
Chromosomes, Human, Pair 5
/
Chromosomes, Human, Pair 8
/
Proto-Oncogene Proteins
/
Heart Defects, Congenital
/
Intellectual Disability
Limits:
Adult
/
Animals
/
Humans
/
Male
Language:
En
Journal:
Eur J Hum Genet
Journal subject:
GENETICA MEDICA
Year:
2009
Document type:
Article
Affiliation country:
Denmark
Country of publication:
United kingdom