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25. A novel mutation in the MSX2 homeobox gene of a family with foramina parietalia permagna, headache and vascular anomaly. Ghassibé M; Bernier V; Boon LM; Vikkula M Eur J Pediatr; 2006 Oct; 165(10):734-5. PubMed ID: 16642368 [No Abstract] [Full Text] [Related]
26. [2 cases of foramina parietalia permagna occurring in the same family]. Okuda O; Ikutomi H No To Shinkei; 1965 Dec; 17(12):1255-9. PubMed ID: 5899437 [No Abstract] [Full Text] [Related]
28. [Familial incidence of foramina parietalia permagna]. Antoni P Orv Hetil; 1967; 108(37):1753-4. PubMed ID: 6061090 [No Abstract] [Full Text] [Related]
29. [Familial foramina parietalia permagna: five cases in a family (author's transl)]. Kinoshita K; Sunami N No To Shinkei; 1980 May; 32(5):523-31. PubMed ID: 7397033 [No Abstract] [Full Text] [Related]
31. A novel mutation in the MSX2 gene in a family with foramina parietalia permagna (FPP). Spruijt L; Verdyck P; Van Hul W; Wuyts W; de Die-Smulders C Am J Med Genet A; 2005 Nov; 139(1):45-7. PubMed ID: 16222674 [No Abstract] [Full Text] [Related]
32. Foramina parietalia permagna in a Nigerian family. Bello TO; Bajomo AA; Adeniyi TO West Afr J Med; 2009 May; 28(3):182-4. PubMed ID: 20306736 [TBL] [Abstract][Full Text] [Related]
33. Syndromal foramina parietalia permagna: "new" or FG syndrome? Comments on the paper by Chrzanowska et al [1998]. Rauch A; Opitz JM; Walker D Am J Med Genet; 1998 Aug; 78(5):406-7. PubMed ID: 9714004 [No Abstract] [Full Text] [Related]
34. The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500). Wuyts W; Cleiren E; Homfray T; Rasore-Quartino A; Vanhoenacker F; Van Hul W J Med Genet; 2000 Dec; 37(12):916-20. PubMed ID: 11106354 [TBL] [Abstract][Full Text] [Related]
35. Identification of mutations in the MSX2 homeobox gene in families affected with foramina parietalia permagna. Wuyts W; Reardon W; Preis S; Homfray T; Rasore-Quartino A; Christians H; Willems PJ; Van Hul W Hum Mol Genet; 2000 May; 9(8):1251-5. PubMed ID: 10767351 [TBL] [Abstract][Full Text] [Related]
36. A case of an extremely large accessory bone with unusual sutures and foramina parietalia permagna in multiple premature craniosynostoses. Hanninger SE; Schwabegger AH J Craniomaxillofac Surg; 2012 Oct; 40(7):555-8. PubMed ID: 22075323 [TBL] [Abstract][Full Text] [Related]