-
1
-
-
0000582294
-
The emissary foramina of the cranium in man and the anthropoids
-
Boyd GI (1930) The emissary foramina of the cranium in man and the anthropoids. J Anat, 65: 108-121.
-
(1930)
J Anat
, vol.65
, pp. 108-121
-
-
Boyd, G.I.1
-
2
-
-
40449106604
-
Complete cranium bifidum without scalp abnormality: Case report
-
DOI 10.3171/PED/2008/1/3/258
-
Celik SE, Kara A (2008) Complete cranium bifidum without scalp abnormality. J Neurosurg Pediatr, 1: 258-260. (Pubitemid 351346518)
-
(2008)
Journal of Neurosurgery: Pediatrics
, vol.1
, Issue.3
, pp. 258-260
-
-
Celik, S.E.1
Kara, A.2
-
3
-
-
0038449055
-
Congenital parietal foramina associated with faulty ossification of the clavicles
-
Eckstein HB, Hoare RD (1963) Congenital parietal foramina associated with faulty ossification of the clavicles. Br J Radiol; 36: 220-221.
-
(1963)
Br J Radiol
, vol.36
, pp. 220-221
-
-
Eckstein, H.B.1
Hoare, R.D.2
-
4
-
-
33747440750
-
Enlarged parietal foramina: MR imaging features in the fetus and neonate
-
Fink AM, Maixner W (2006) Enlarged parietal foramina: MR imaging features in the fetus and neonate. Am J Neuroradiol, 27: 1379-1381. (Pubitemid 44897662)
-
(2006)
American Journal of Neuroradiology
, vol.27
, Issue.6
, pp. 1379-1381
-
-
Fink, A.M.1
Maixner, W.2
-
5
-
-
0002537849
-
"The catlin mark" the inheritance of an unusual opening in the parietal bone
-
Goldsmith WM (1922) "The catlin mark" the inheritance of an unusual opening in the parietal bone. J Hered, 13: 69-71.
-
(1922)
J Hered
, vol.13
, pp. 69-71
-
-
Goldsmith, W.M.1
-
7
-
-
40449086960
-
On congenital and symmetrical perforation of both parietal bones
-
Greig DM (1892) On congenital and symmetrical perforation of both parietal bones. J Anat Physiol, 26: 187-191.
-
(1892)
J Anat Physiol
, vol.26
, pp. 187-191
-
-
Greig, D.M.1
-
9
-
-
84872208561
-
-
Huber cited by Rahilly et al. 1952 - [18]
-
Huber cited by Rahilly et al. 1952 - [18].
-
-
-
-
10
-
-
0014443035
-
A concordant craniofacial dysostosis with Enlarged parietal Foramina in twins
-
Lehrer HZ, Familant JW (1969) A concordant craniofacial dysostosis with Enlarged parietal Foramina in twins. Radiology, 92: 127-129.
-
(1969)
Radiology
, vol.92
, pp. 127-129
-
-
Lehrer, H.Z.1
Familant, J.W.2
-
11
-
-
0025307712
-
Hereditary cranium bifidum and symmetric parietal foramina are the same entity
-
Little BB, Knoll KA, Klein VR, Heller KB (1990) Hereditary cranium bifidum and symmetric parietal foramina are the same entity. Am J Med Genet, 35: 453-458. (Pubitemid 20109001)
-
(1990)
American Journal of Medical Genetics
, vol.35
, Issue.4
, pp. 453-458
-
-
Little, B.B.1
Knoll, K.A.2
Klein, V.R.3
Heller, K.B.4
-
12
-
-
0025099424
-
Enlarged parietal foramina and craniosynostosis in an American Indian child
-
Mann RW (1990) Enlarged parietal foramina and craniosynostosis in an American Indian child. Am J Rad, 154: 658. (Pubitemid 20071640)
-
(1990)
American Journal of Roentgenology
, vol.154
, Issue.3
, pp. 658
-
-
Mann, R.W.1
-
13
-
-
31344446614
-
Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: From genotype to phenotype
-
DOI 10.1038/sj.ejhg.5201526, PII 5201526
-
Mavrogiannis LA, Taylor IB, Davies SJ, Ramos FJ, Olivares JL, Wilkie AOM (2006) Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype. Eur J Hum Genetics, 14: 151-158. (Pubitemid 43135857)
-
(2006)
European Journal of Human Genetics
, vol.14
, Issue.2
, pp. 151-158
-
-
Mavrogiannis, L.A.1
Taylor, I.B.2
Davies, S.J.3
Ramos, F.J.4
Olivares, J.L.5
Wilkie, A.O.M.6
-
15
-
-
0014873914
-
Evolution of persistently enlarged parietal foramina
-
Murphy J, Gooding CA (1970) Evolution of persistently enlarged parietal foramina. Radiology, 97: 391-392.
-
(1970)
Radiology
, vol.97
, pp. 391-392
-
-
Murphy, J.1
Gooding, C.A.2
-
16
-
-
0029067515
-
Aplasia cutis congenital and enlarged parietal foramina (Catlin marks)
-
Preis S, Engelbrecht V, Lenard HG (1995) Aplasia cutis congenital and enlarged parietal foramina (Catlin marks). Acta Paediatr, 84: 701-702.
-
(1995)
Acta Paediatr
, vol.84
, pp. 701-702
-
-
Preis, S.1
Engelbrecht, V.2
Lenard, H.G.3
-
17
-
-
0042604847
-
Hereditary occrence of enlarged parietal foramina
-
cited by Hollender 1967 - [8]
-
Pepper OH, Pendergrass EP (1936) Hereditary occrence of enlarged parietal foramina. Am J Roentgenol Rad Therapy, 35: 1-8 (cited by Hollender 1967 - [8]).
-
(1936)
Am J Roentgenol Rad Therapy
, vol.35
, pp. 1-8
-
-
Pepper, O.H.1
Pendergrass, E.P.2
-
18
-
-
0344522622
-
Foramina parietalia permagna
-
Rahilly RO, Twohig MJ (1952) Foramina parietalia permagna. Am J Radiol, 67: 551-561.
-
(1952)
Am J Radiol
, vol.67
, pp. 551-561
-
-
Rahilly, R.O.1
Twohig, M.J.2
-
19
-
-
0034646234
-
Enlarged parietal foramina: Association with cerebral venous and cortical anomalies
-
Reddy AT, Hedlund GL, Percy AK (2000) Neurology. Enlarged parietal foramina: association with cerebral venous and cortical anomalies. Neurology, 54: 1175-1178. (Pubitemid 30151864)
-
(2000)
Neurology
, vol.54
, Issue.5
, pp. 1175-1178
-
-
Reddy, A.T.1
Hedlund, G.L.2
Percy, A.K.3
-
20
-
-
0343745129
-
Congenital perforations of the skull in relation to parietal bone
-
cited by Hollender 1967 - [8]
-
Robinsons RG (1962) Congenital perforations of the skull in relation to parietal bone. J Neurosurg, 19: 153 (cited by Hollender 1967 - [8]).
-
(1962)
J Neurosurg
, vol.19
, pp. 153
-
-
Robinsons, R.G.1
-
21
-
-
84872204239
-
-
Toldt cited by Rahilly et al. 1952 - [18]
-
Toldt cited by Rahilly et al. 1952 - [18].
-
-
-
-
22
-
-
0141679613
-
Parietal foramina are not synonymous with giant parietal foramina
-
DOI 10.1159/000072475
-
Tubbs RS, Smyth MD, Oakes WJ (2003) Parietal foramina are not synonymous with giant parietal foramina. Pediatr Neurosurg, 39: 216-217. (Pubitemid 37116990)
-
(2003)
Pediatric Neurosurgery
, vol.39
, Issue.4
, pp. 216-217
-
-
Tubbs, R.S.1
Smyth, M.D.2
Oakes, W.J.3
-
24
-
-
0034530307
-
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 (2000) The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500). Med Genet, 37: 916-920. (Pubitemid 32002887)
-
(2000)
Journal of Medical Genetics
, vol.37
, Issue.12
, pp. 916-920
-
-
Wuyts, W.1
Cleiren, E.2
Homfray, T.3
Rasore-Quartino, A.4
Vanhoenacker, F.5
Van Hul, W.6
|