De novo translocation (2;18)(q21;q22) in a child with severe epilepsy, developmental delay and mild dysmorphism.
Genet Couns
; 11(3): 221-7, 2000.
Article
in En
| MEDLINE
| ID: mdl-11043430
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Translocation, Genetic
/
Chromosomes, Human, Pair 2
/
Chromosomes, Human, Pair 18
/
Developmental Disabilities
/
Epilepsy
/
Face
Limits:
Humans
/
Infant
/
Male
Language:
En
Journal:
Genet Couns
Journal subject:
ETICA
/
GENETICA MEDICA
Year:
2000
Document type:
Article
Affiliation country:
Netherlands