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Paediatric phenotype of Kallmann syndrome due to mutations of fibroblast growth factor receptor 1 (FGFR1)
PaperCitations, authors & open-access status
Paediatric phenotype of Kallmann syndrome due to mutations of fibroblast growth factor receptor 1 (FGFR1) is a paper indexed in ScholarIQ from OpenAlex. ScholarIQ records 55 citations, 2006 year and closed oa status.
55
Citations
2006
Year
closed
OA Status