Distinct phenotype associated with a cryptic subtelomeric deletion of 19p13.3-pter.

Archer, H L

Distinct phenotype associated with a cryptic subtelomeric deletion of 19p13.3-pter. [electronic resource] - American journal of medical genetics. Part A Jul 2005 - 38-44 p. digital

Publication Type: Case Reports; Journal Article; Review

1552-4825

10.1002/ajmg.a.30774 doi


Abnormalities, Multiple--genetics
Adolescent
Chromosome Deletion
Chromosomes, Human, Pair 19--genetics
Cleft Palate--pathology
Face--abnormalities
Genetic Predisposition to Disease--genetics
Hearing Loss--pathology
Heart Defects, Congenital--pathology
Humans
Immune System--abnormalities
In Situ Hybridization, Fluorescence
Keloid--pathology
Learning Disabilities--pathology
Male
Phenotype
Telomere--genetics