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Loss-of-function mutations in FGFR1 cause autosomal domin... | ResearchHub
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Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome
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Authors
Catherine Dodé
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Catherine Dodé
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Catherine Dodé
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Jean‐Pierre Hardelin
Published
March 10, 2003
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Journal
Nature Genetics
Topics
Biology
Internal Medicine
Medicine
Endocrinology
Molecular Biology
Show all topics
DOI
10.1038/ng1122
