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. Author manuscript; available in PMC: 2014 May 6.
Published in final edited form as: Mol Cell Endocrinol. 2013 Mar 14;370(0):138–148. doi: 10.1016/j.mce.2013.02.016

Fig. 1.

Fig. 1

Pedigree of the family with four affected nHH patients with compound heterozygous GNRHR mutations denoted by shaded squares or circles. Female patient II-8 has delayed puberty, but the genotype is unknown. Modified from Layman et al. (1998).