TY  - GEN
AU  - Gulati,Reena
AU  - Verdin,Hannah
AU  - Halanaik,Dhanapathi
AU  - Bhat,B Vishnu
AU  - De Baere,Elfride
TI  - Co-occurrence of congenital hydronephrosis and FOXL2-associated blepharophimosis, ptosis, epicanthus inversus syndrome (BPES)
SN  - 1878-0849
PY  - 2015///0612
KW  - Adult
KW  - Blepharophimosis
KW  - complications
KW  - Child, Preschool
KW  - Fathers
KW  - Forkhead Box Protein L2
KW  - Forkhead Transcription Factors
KW  - genetics
KW  - Humans
KW  - Hydronephrosis
KW  - Male
KW  - Mutation
KW  - Phenotype
KW  - Skin Abnormalities
KW  - Urogenital Abnormalities
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/j.ejmg.2014.08.004
ER  -