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Items: 1 to 20 of 243

1.

Syndromic foramina parietalia permagna.

Chrzanowska K, Kozlowski K, Kowalska A.

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

PMID:
9714003
2.

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 6;78(5):406-7. No abstract available.

PMID:
9714004
3.

[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
4.

The Robinow syndrome: an isolated case with a detailed study of the phenotype.

Kelly TE, Benson R, Temtamy S, Plotnick L, Levin S.

Am J Dis Child. 1975 Mar;129(3):383-6. No abstract available.

PMID:
1121970
5.

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
6.

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
7.

[Foramina parietalia permagna].

Solymosi L, Leuwer S, Wappenschmidt J.

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

PMID:
3671717
8.

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
9.

[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.

10.

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
11.

[Familial incidence of foramina parietalia permagna].

Antoni P.

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

PMID:
6061090
12.

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
13.

[Foramina parietalia permagna: case report].

Nikolić S, Živković V, Strajina V.

Srp Arh Celok Lek. 2012 Sep-Oct;140(9-10):658-61. Serbian.

14.

[Associated malformations of the head and extremities].

Tridon P.

J Genet Hum. 1974 Dec;22(4):365-80. French. No abstract available.

PMID:
4282383
15.

Surgical management of foramina parietalia permagna.

Kortesis B, Richards T, David L, Glazier S, Argenta L.

J Craniofac Surg. 2003 Jul;14(4):538-44.

PMID:
12867871
16.

Rubinstein-Taybi syndrome.

Berry AC.

J Med Genet. 1987 Sep;24(9):562-6. Review. No abstract available.

17.

[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
18.

[Foramina parietalia permagna. Case report].

Esposito M.

Radiol Med. 1967 Oct;53(10):987-91. Italian. No abstract available.

PMID:
5192126
19.

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
20.

Congenital heart disease in an infant with the Smith-Lemli-Opitz syndrome.

Park SC, Needles CF, Dimich I, Sussman L.

J Pediatr. 1968 Dec;73(6):896-902. No abstract available.

PMID:
4386913
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