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FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome. [electronic resource] by
- Kriederman, Benjamin M
- Myloyde, Teressa L
- Witte, Marlys H
- Dagenais, Susan L
- Witte, Charles L
- Rennels, Margaret
- Bernas, Michael J
- Lynch, Michelle T
- Erickson, Robert P
- Caulder, Mark S
- Miura, Naoyuki
- Jackson, David
- Brooks, Brian P
- Glover, Thomas W
Producer: 20040211
In:
Human molecular genetics vol. 12
Availability: No items available.
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