TY  - GEN
AU  - Archer,H L
AU  - Gupta,S
AU  - Enoch,S
AU  - Thompson,P
AU  - Rowbottom,A
AU  - Chua,I
AU  - Warren,S
AU  - Johnson,D
AU  - Ledbetter,D H
AU  - Lese-Martin,C
AU  - Williams,P
AU  - Pilz,D T
TI  - Distinct phenotype associated with a cryptic subtelomeric deletion of 19p13.3-pter
SN  - 1552-4825
PY  - 2005///0810
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Adolescent
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 19
KW  - Cleft Palate
KW  - pathology
KW  - Face
KW  - abnormalities
KW  - Genetic Predisposition to Disease
KW  - Hearing Loss
KW  - Heart Defects, Congenital
KW  - Humans
KW  - Immune System
KW  - In Situ Hybridization, Fluorescence
KW  - Keloid
KW  - Learning Disabilities
KW  - Male
KW  - Phenotype
KW  - Telomere
N1  - Publication Type: Case Reports; Journal Article; Review
UR  - https://doi.org/10.1002/ajmg.a.30774
ER  -