TY  - GEN
AU  - Lennon,P A
AU  - Scott,D A
AU  - Lonsdorf,D
AU  - Wargowski,D S
AU  - Kirkpatrick,S
AU  - Patel,A
AU  - Cheung,S W
TI  - WAGR(O?) syndrome and congenital ptosis caused by an unbalanced t(11;15)(p13;p11.2)dn demonstrating a 7 megabase deletion by FISH
SN  - 1552-4825
PY  - 2006///0727
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Blepharoptosis
KW  - pathology
KW  - Chromosome Banding
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 11
KW  - Chromosomes, Human, Pair 15
KW  - Female
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Infant
KW  - Karyotyping
KW  - Obesity
KW  - Translocation, Genetic
KW  - WAGR Syndrome
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1002/ajmg.a.31229
ER  -