TY  - GEN
AU  - Uhlenhaut,Nina Henriette
AU  - Treier,Mathias
TI  - Foxl2 function in ovarian development
SN  - 1096-7192
PY  - 2006///0925
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Amino Acid Sequence
KW  - Animals
KW  - Blepharophimosis
KW  - Blepharoptosis
KW  - Evolution, Molecular
KW  - Eyelids
KW  - abnormalities
KW  - Female
KW  - Forkhead Box Protein L2
KW  - Forkhead Transcription Factors
KW  - Humans
KW  - Infertility, Female
KW  - Mice
KW  - Molecular Sequence Data
KW  - Mutation
KW  - Ovary
KW  - Primary Ovarian Insufficiency
KW  - Regulatory Elements, Transcriptional
KW  - Syndrome
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review
UR  - https://doi.org/10.1016/j.ymgme.2006.03.005
ER  -