| 1 | SSPS, WNT10A |
| Intra-familial variability of ectodermal defects associated with WNT10A mutations. | |
| Wedgeworth EK, Nagy N, White JM, Pembroke AC, McGrath JA. | |
| Acta Derm Venereol 91(3):346-7. doi: 10.2340/00015555-1028. No abstract available. 2011 | |
| 2 | SSPS, WNT10A |
| WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes. | |
| Bohring A, Stamm T, Spaich C, Haase C, Spree K, Hehr U, Hoffmann M, Ledig S, Sel S, Wieacker P, Röpke A. | |
| Am J Hum Genet 85(1):97-105. Epub 2009 Jun 25. 2009 | |
| 3 | SSPS |
| Schöpf-Schulz-Passarge syndrome with an unusual pattern of inheritance. | |
| Craigen WJ, Levy ML, Lewis RA. | |
| Am J Med Genet 71(2):186-8. 1997 | |