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Mutations in FOXC2 (MFH-1), a Forkhead Family Transcription Factor, Are Responsible for the Hereditary Lymphedema-Distichiasis Syndrome

✍ Scribed by Jianming Fang; Susan L. Dagenais; Robert P. Erickson; Martin F. Arlt; Michael W. Glynn; Jerome L. Gorski; Laurie H. Seaver; Thomas W. Glover


Book ID
117853473
Publisher
American Society of Human Genetics
Year
2000
Tongue
English
Weight
583 KB
Volume
67
Category
Article
ISSN
0002-9297

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