Familial kallmann’s syndrome with autosomal dominant inheritance, variable gonadotropin deficiency and subtle color vision defects

Arieh Kauschansky*, L. Everett Seyler, Lawrence E. Marks, William S. Cain, Myron Genel

*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

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Biochemistry, Genetics and Molecular Biology

Neuroscience