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Items: 1 to 20 of 156

1.

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 15;139(1):45-7. No abstract available.

PMID:
16222674
2.

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. Epub 2006 Apr 27. No abstract available.

PMID:
16642368
3.

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 1;9(8):1251-5.

4.

Foramina parietalia permagna: the ins and outs.

Dharwal K.

Folia Morphol (Warsz). 2012 May;71(2):78-81.

PMID:
22648584
5.

Prenatal sonographic appearance of foramina parietalia permagna.

Salamanca A, Gonzalez-Gomez F, Padilla MC, Motos MA, Zorrilla F, Sabatel RM.

Prenat Diagn. 1994 Aug;14(8):766-9.

PMID:
7991518
6.

Foramina parietalia permagna: report of nine cases in one family.

Kutilek S, Baxova A, Bayer M, Leiska A, Kozlowski K.

J Paediatr Child Health. 1997 Apr;33(2):168-70.

PMID:
9145364
7.

Parietal foramina with cleidocranial dysplasia is caused by mutation in MSX2.

Garcia-Miñaur S, Mavrogiannis LA, Rannan-Eliya SV, Hendry MA, Liston WA, Porteous ME, Wilkie AO.

Eur J Hum Genet. 2003 Nov;11(11):892-5.

8.

Parietal bone agenesis and associated multiple congenital anomalies.

de Heer IM, van Nesselrooij BP, Spliet W, Vermeij-Keers C.

J Craniofac Surg. 2003 Mar;14(2):192-6.

PMID:
12621289
9.

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.

10.

Hereditary enlarged parietal foramina (foramina parietalia permagna). Prenatal diagnosis, evolution and family study.

Rasore-Quartino A, Vignola G, Camera G.

Pathologica. 1985 Jul-Aug;77(1050):449-55. No abstract available.

PMID:
3834376
11.

Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification.

Wilkie AO, Tang Z, Elanko N, Walsh S, Twigg SR, Hurst JA, Wall SA, Chrzanowska KH, Maxson RE Jr.

Nat Genet. 2000 Apr;24(4):387-90.

PMID:
10742103
12.

Syndromic foramina parietalia permagna.

Chrzanowska K, Kozlowski K, Kowalska A.

Am J Med Genet. 1998 Aug 6;78(5):401-5.

PMID:
9714003
13.

[Foramina parietalia permagna].

Solymosi L, Leuwer S, Wappenschmidt J.

Radiologe. 1987 Jun;27(6):269-72. German.

PMID:
3671717
14.

[Foramina parietalia permagna, an uncommon congenital defect].

Blanco del Val A, Carrascal Arranz MI, Centeno Malfaz F, Marcos Andrés H, Alcalde Martín C.

An Pediatr (Barc). 2003 May;58(5):506-7. Spanish. No abstract available.

15.

[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. Japanese. No abstract available.

PMID:
7397033
16.

Epilepsy in one family with parietal foramina: an incidental finding?

Valente KD, Valente M.

J Neurol Neurosurg Psychiatry. 2004 Nov;75(11):1648-9. No abstract available.

17.

[Rare congenital developmental anomaly of the skull: foramina parietalia permagna].

Kaposi PN.

Rofo. 1982 Aug;137(2):229-30. German. No abstract available.

PMID:
6215312
18.

[Familial incidence of foramina parietalia permagna].

Antoni P.

Orv Hetil. 1967;108(37):1753-4. Hungarian. No abstract available.

PMID:
6061090
19.

Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype.

Mavrogiannis LA, Taylor IB, Davies SJ, Ramos FJ, Olivares JL, Wilkie AO.

Eur J Hum Genet. 2006 Feb;14(2):151-8.

20.

[2 cases of foramina parietalia permagna occurring in the same family].

Okuda O, Ikutomi H.

No To Shinkei. 1965 Dec;17(12):1255-9. Japanese. No abstract available.

PMID:
5899437
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