Cortically Evoked Motor Responses in Patients with Xp22. 3-Linked Kallmann's Syndrome and in Female Gene Carriers
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Brief Report:Intragenic Deletion of the Kalig-1 Gene in Kallmann's Syndrome
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Neurologic Findings in Men with Isolated Hypogonadotropic Hypogonadism
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Developmental Learning Disabilities of the Right Hemisphere
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