A de novo 1.1-1.6 Mb subtelomeric deletion of chromosome 20q13.33 in a patient with learning difficulties but without obvious dysmorphic features.

Béna, Frédérique

A de novo 1.1-1.6 Mb subtelomeric deletion of chromosome 20q13.33 in a patient with learning difficulties but without obvious dysmorphic features. [electronic resource] - American journal of medical genetics. Part A Aug 2007 - 1894-9 p. digital

Publication Type: Case Reports; Journal Article

1552-4825

10.1002/ajmg.a.31789 doi


Child, Preschool
Chromosome Deletion
Chromosomes, Human, Pair 20
Face--abnormalities
Female
Humans
In Situ Hybridization, Fluorescence
Learning Disabilities--genetics
Oligonucleotide Array Sequence Analysis
Strabismus--diagnosis
Telomere--genetics