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. Author manuscript; available in PMC: 2014 Feb 7.
Published in final edited form as: Hum Mutat. 2011 Sep 29;32(12):1417–1426. doi: 10.1002/humu.21590

Figure 1.

Figure 1

Pedigrees of Irish Traveller families with MCOPCB. (A–C) The inheritance pattern in each pedigree is compatible with an autosomal recessive disease gene. Pedigrees 1–3 are from the Irish Traveller population but are unrelated to each other. A: DNA samples were available for 6 affected and 7 unaffected family members in pedigree 1. B: DNA was available for the affected proband and his parents in pedigree 2. C: The female proband in pedigree 3 was diagnosed with Matthew-Wood syndrome (MWS). Her elder brother had bilateral anophthalmia only and no other clinical features. DNA was available for the MWS patient.