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Mutations in FOXC2 (MFH-1), a Forkhead Family Transcripti... | ResearchHub
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Mutations in FOXC2 (MFH-1), a Forkhead Family Transcription Factor, Are Responsible for the Hereditary Lymphedema-Distichiasis Syndrome
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Authors
Jianming Fang
7 more
Jianming Fang
•
Susan Dagenais
5 more
•
Thomas Glover
Published
December 1, 2000
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Journal
The American Journal of Human Genetics
Topics
Biology
Cancer Oncology
Cell Biology
Phenotype
Breakpoint
Show all topics
DOI
10.1086/316915
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publisher-specific-oa
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Journal
The American Journal of Human Genetics
Topics
Biology
Cancer Oncology
Cell Biology
Phenotype
Breakpoint
Show all topics
DOI
10.1086/316915
License
publisher-specific-oa
