Towards mapping phenotypical traits in 18p- syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation.

Brenk, Christian H

Towards mapping phenotypical traits in 18p- syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation. [electronic resource] - European journal of human genetics : EJHG Jan 2007 - 35-44 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

1018-4813

10.1038/sj.ejhg.5201718 doi


Adolescent
Adult
Child, Preschool
Chromosome Breakage
Chromosome Deletion
Chromosome Mapping
Chromosomes, Human, Pair 18
Chromosomes, Human, Pair 20
Face
Female
Humans
In Situ Hybridization, Fluorescence
Intellectual Disability--genetics
Karyotyping
Male
Phenotype
Syndrome
Translocation, Genetic