Article
Terminal deletion of chromosome 10q26: delineation of two clinical phenotypes.
Genetic counseling (Geneva, Switzerland) - 1 Jan 1998
Petit P, Devriendt K, Azou M, Gewillig M, Fryns J P
Abstract excerpt
We present genotype-phenotype correlations in two patients with distal 10q deletion. A patient with a small terminal deletion presented mild mental retardation and behavioral difficulties with hyperactivity, whereas the patient with a larger deletion, had multiple congenital anomalies and moderat...
Topics
- Abnormalities, Multiple
- Attention Deficit and Disruptive Behavior Disorders
- Child
- Chromosome Deletion
- Chromosomes, Human, Pair 10
- Female
- Genotype
- Humans
- In Situ Hybridization, Fluorescence
- Intellectual Disability
- Karyotyping
- Male
- Microcephaly
- Phenotype