NAHR-mediated copy-number variants in a clinical population: mechanistic insights into both genomic disorders and Mendelizing traits.
Genome Res
; 23(9): 1395-409, 2013 Sep.
Article
in En
| MEDLINE
| ID: mdl-23657883
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Chromosome Disorders
/
Alleles
/
DNA Copy Number Variations
/
Homologous Recombination
/
Genetic Diseases, Inborn
Limits:
Humans
Language:
En
Journal:
Genome Res
Journal subject:
BIOLOGIA MOLECULAR
/
GENETICA
Year:
2013
Document type:
Article
Affiliation country:
United States
Country of publication:
United States