Kauschansky,, Arieh, Seyler,, L. Everett, Marks,, Lawrence E., Cain,, William S. and Genel,, Myron. "FAMILIAL KALLMANN'S SYNDROME WITH AUTOSOMAL DOMINANT INHERITANCE, VARIABLE GONADOTROPIN DEFICIENCY AND SUBTLE COLOR VISION DEFECTS"
International Journal of Adolescent Medicine and Health, vol. 2, no. 2, 1986, pp. 81-98.
https://doi.org/10.1515/IJAMH.1986.2.2.81Kauschansky,, A., Seyler,, L., Marks,, L., Cain,, W. & Genel,, M. (1986). FAMILIAL KALLMANN'S SYNDROME WITH AUTOSOMAL DOMINANT INHERITANCE, VARIABLE GONADOTROPIN DEFICIENCY AND SUBTLE COLOR VISION DEFECTS.
International Journal of Adolescent Medicine and Health,
2(2), 81-98.
https://doi.org/10.1515/IJAMH.1986.2.2.81Kauschansky,, A., Seyler,, L., Marks,, L., Cain,, W. and Genel,, M. (1986) FAMILIAL KALLMANN'S SYNDROME WITH AUTOSOMAL DOMINANT INHERITANCE, VARIABLE GONADOTROPIN DEFICIENCY AND SUBTLE COLOR VISION DEFECTS. International Journal of Adolescent Medicine and Health, Vol. 2 (Issue 2), pp. 81-98.
https://doi.org/10.1515/IJAMH.1986.2.2.81Kauschansky,, Arieh, Seyler,, L. Everett, Marks,, Lawrence E., Cain,, William S. and Genel,, Myron. "FAMILIAL KALLMANN'S SYNDROME WITH AUTOSOMAL DOMINANT INHERITANCE, VARIABLE GONADOTROPIN DEFICIENCY AND SUBTLE COLOR VISION DEFECTS"
International Journal of Adolescent Medicine and Health 2, no. 2 (1986): 81-98.
https://doi.org/10.1515/IJAMH.1986.2.2.81Kauschansky, A, Seyler, L, Marks, L, Cain, W, Genel, M. FAMILIAL KALLMANN'S SYNDROME WITH AUTOSOMAL DOMINANT INHERITANCE, VARIABLE GONADOTROPIN DEFICIENCY AND SUBTLE COLOR VISION DEFECTS.
International Journal of Adolescent Medicine and Health. 1986;2(2): 81-98.
https://doi.org/10.1515/IJAMH.1986.2.2.81Copied to clipboard
