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. 2023 Feb 8;8(3):e164324. doi: 10.1172/jci.insight.164324

Figure 1. Family pedigrees of probands with SOX2 variants identified in the Massachusetts General Hospital IHH cohort.

Figure 1

Probands are identified by arrows; + indicates wild-type (WT) allele; and V indicates the variant allele. FGFR1, FGF receptor 1; KS, Kallmann syndrome; nIHH, normosmic IHH.