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Loss-of-function mutations in FGFR1 cause autosomal domin... | ResearchHub

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Journal

Nature Genetics

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Internal Medicine

Molecular Biology

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Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome

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Authors

Catherine Dodé

Catherine Dodé•Catherine Dodé•Jean‐Pierre Hardelin

Published

March 10, 2003

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Journal

Nature Genetics

Topics

Internal Medicine

Molecular Biology

DOI