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. Author manuscript; available in PMC: 2015 Feb 1.
Published in final edited form as: Nat Genet. 2008 Dec 11;41(3):354–358. doi: 10.1038/ng.306

Figure 1.

Figure 1

A. Families used to identify critical interval on chromosome 4 harbouring genetic defect causing nIHH B. Critical region on chromosome 4 showing homozygosity (black) in all affected individuals, with known or predicted genes in region indicated. C. Location of pathogenic mutation in NK3R D. evolutionary conservation of mutated residues.