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Kallmann syndrome. From genetics to neurobiology

8 Dec 1993

Abstract excerpt

IN THE last few years, numerous discoveries in the field of human genetics have had a significant impact both on medical practice and on basic science. Kallmann syndrome represents the first human disease caused by a neuronal migration defect for which the gene has been identified and is a good example of how genetics has permitted the integration of clinical observation with developmental biology, contributing...

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PMID: 8133589
DOI: 10.1001/jama.270.22.2713

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