| 1 | ALX4, DEL11PP, MSX2, PFM1, PFM2
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| Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype.
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| Mavrogiannis LA, Taylor IB, Davies SJ, Ramos FJ, Olivares JL, Wilkie AO.
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| Eur J Hum Genet 14(2):151-8. 2006
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| 2 | ALX4, PFM1, MNX1, SCRA, VSX1, KTCN1, VSX2, MCIA, SOPT, HESX1, HOXD13, PSDY2, MSX2, PFM2, SIX3, HPE2, DCS, SHOX
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| Homeodomain revisited: a lesson from disease-causing mutations.
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| Chi YI.
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| Hum Genet 116(6):433-44. Epub 2005 Feb 23. 2005
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| 3 | MSX2, PFM2
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| A novel mutation in the MSX2 gene in a family with foramina parietalia permagna (FPP).
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| Spruijt L, Verdyck P, Van Hul W, Wuyts W, de Die-Smulders C.
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| Am J Med Genet A 139A(1):45-47. 2005
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| 4 | ALX4, MSX2, PFM1, PFM2
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| Alx4 and Msx2 play phenotypically similar and additive roles in skull vault differentiation.
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| Antonopoulou I, Mavrogiannis LA, Wilkie AO, Morriss-Kay GM.
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| J Anat 204(6):487-99.
2004
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| 5 | MSK2, PFM2
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| Parietal foramina with cleidocranial dysplasia is caused by mutation in MSX2.
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| Garcia-Miņaur S, Mavrogiannis LA, Rannan-Eliya SV, Hendry MA, Liston WA, Porteous ME, Wilkie AO.
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| Eur J Hum Genet 11(11):892-5.
2003
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| 6 | MSX2, PFM2
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| Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification.
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| Wilkie AO, Tang Z, Elanko N, Walsh S, Twigg SR, Hurst JA, Wall SA, Chrzanowska KH, Maxson RE Jr.
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| Nat Genet 24(4):387-90. 2000
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| 7 | MSX2, PFM2
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| Identification of mutations in the MSX2 homeobox gene in families affected with foramina parietalia permagna.
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| Wuyts W, Reardon W, Preis S, Homfray T, Rasore-Quartino A, Christians H, Willems PJ, Van Hul W.
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| Hum Mol Genet 9(8):1251-5. 2000
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