-
1
-
-
0025166503
-
The Schinzel-Giedion syndrome
-
Al-Gazali LI, Farndon P, Burn J, Flannery DB, Davison C, Mueller RF (1990): The Schinzel-Giedion syndrome. J Med Genet 27: 42-47.
-
(1990)
J Med Genet
, vol.27
, pp. 42-47
-
-
Al-Gazali, L.I.1
Farndon, P.2
Burn, J.3
Flannery, D.B.4
Davison, C.5
Mueller, R.F.6
-
2
-
-
9344224039
-
Mittelgesichtshypoplasie, Skelettanomalien, Apnoen, Retardierung-eine weitere Beobachtung
-
Tolksdorf M, Spranger J (eds): in Kiel, Jahrgang 8
-
Burck U (1982): Mittelgesichtshypoplasie, Skelettanomalien, Apnoen, Retardierung-eine weitere Beobachtung. In Tolksdorf M, Spranger J (eds): "Klinische Genetik in der Pediatrie." 3 Symposium, in Kiel, Jahrgang 8, Heft 5.
-
(1982)
"Klinische Genetik in der Pediatrie." 3 Symposium
, Issue.5
-
-
Burck, U.1
-
3
-
-
0018562452
-
A further case of a new syndrome including midface retraction, hypertrichosis and skeletal anomalies
-
Donnai D, Harris R (1979): A further case of a new syndrome including midface retraction, hypertrichosis and skeletal anomalies. J Med Genet 16: 483-486.
-
(1979)
J Med Genet
, vol.16
, pp. 483-486
-
-
Donnai, D.1
Harris, R.2
-
4
-
-
0010735902
-
Schinzel-Giedion syndrome: Report of the fifth case
-
Hall B (1989): Schinzel-Giedion syndrome: report of the fifth case. Proc Greenwood Genet Cen 9: 113-114.
-
(1989)
Proc Greenwood Genet Cen
, vol.9
, pp. 113-114
-
-
Hall, B.1
-
6
-
-
0020473059
-
Congenital hydronephrosis, skeletal dysplasia, and severe developmental retardation: The Schinzel Giedion syndrome
-
Kelly RI, Zackai EH, Charney EB (1982): Congenital hydronephrosis, skeletal dysplasia, and severe developmental retardation: the Schinzel Giedion syndrome. J Pediatr 100: 943-946.
-
(1982)
J Pediatr
, vol.100
, pp. 943-946
-
-
Kelly, R.I.1
Zackai, E.H.2
Charney, E.B.3
-
7
-
-
0028265081
-
Three new cases of the Schinzel-Giedion syndrome and review of the literature
-
Labrune P, Lyonnet S, Zupan V, Imbert M-C, Goutieres F, Hubert P, Le Merrer M (1994): Three new cases of the Schinzel-Giedion syndrome and review of the literature. Am J Med Genet 50: 90-93.
-
(1994)
Am J Med Genet
, vol.50
, pp. 90-93
-
-
Labrune, P.1
Lyonnet, S.2
Zupan, V.3
Imbert, M.-C.4
Goutieres, F.5
Hubert, P.6
Le Merrer, M.7
-
8
-
-
0010695130
-
Schinzel-Giedion syndrome or Rudiger syndrome: An additional case and discussion
-
Leonard CO (1983): Schinzel-Giedion syndrome or Rudiger syndrome: an additional case and discussion. Proc Greenwood Genet Cen 2: 126.
-
(1983)
Proc Greenwood Genet Cen
, vol.2
, pp. 126
-
-
Leonard, C.O.1
-
9
-
-
0025778874
-
Neurosonography and pathology in the Schinzel-Giedion syndrome
-
Maclennan AC, Doyle D, Simpson RM (1991): Neurosonography and pathology in the Schinzel-Giedion syndrome. J Med Genet 28: 547-549.
-
(1991)
J Med Genet
, vol.28
, pp. 547-549
-
-
Maclennan, A.C.1
Doyle, D.2
Simpson, R.M.3
-
11
-
-
0025344437
-
The Schinzel-Giedion syndrome. A case report and review of the literature
-
Pul M, Yilmaz N, Komsuoglu B (1990): The Schinzel-Giedion syndrome. A case report and review of the literature. Clin Pediatr 29: 235-239.
-
(1990)
Clin Pediatr
, vol.29
, pp. 235-239
-
-
Pul, M.1
Yilmaz, N.2
Komsuoglu, B.3
-
12
-
-
0027525497
-
New finding of Schinzel-Giedion syndrome: A case with a malignant sacrococcygeal teratoma
-
Robin NH, Grace K, DeSouza TG, McDonald-McGinn D, Zackai EH (1993): New finding of Schinzel-Giedion syndrome: a case with a malignant sacrococcygeal teratoma. Am J Med Genet 47: 852-856.
-
(1993)
Am J Med Genet
, vol.47
, pp. 852-856
-
-
Robin, N.H.1
Grace, K.2
DeSouza, T.G.3
McDonald-McGinn, D.4
Zackai, E.H.5
-
13
-
-
0027960156
-
Schinzel-Giedion syndrome: Autopsy report and additional clinical manifestations
-
Rodriguez JI, Jiménez-Heffernan JA, Leal J (1994): Schinzel-Giedion syndrome: autopsy report and additional clinical manifestations. Am J Med Genet 53: 374-377.
-
(1994)
Am J Med Genet
, vol.53
, pp. 374-377
-
-
Rodriguez, J.I.1
Jiménez-Heffernan, J.A.2
Leal, J.3
-
14
-
-
0015177864
-
Severe developmental failure with coarse facial features, distal limb hypoplasia, thickened palmar creases, bifid uvula, and ureteral stenosis: A previously unidentified familial disorder with lethal outcome
-
Rüdiger RA, Schmidt W, Loose DA, Passarge E (1971): Severe developmental failure with coarse facial features, distal limb hypoplasia, thickened palmar creases, bifid uvula, and ureteral stenosis: a previously unidentified familial disorder with lethal outcome. J Pediatr 79: 977-981.
-
(1971)
J Pediatr
, vol.79
, pp. 977-981
-
-
Rüdiger, R.A.1
Schmidt, W.2
Loose, D.A.3
Passarge, E.4
-
16
-
-
0017832764
-
A syndrome of severe midface retraction, multiple skull anomalies, clubfeet, and cardiac and renal malformations in sibs
-
Schinzel A, Giedion A (1978): A syndrome of severe midface retraction, multiple skull anomalies, clubfeet, and cardiac and renal malformations in sibs. Am J Med Genet 1: 361-375.
-
(1978)
Am J Med Genet
, vol.1
, pp. 361-375
-
-
Schinzel, A.1
Giedion, A.2
-
18
-
-
0027178172
-
Schinzel-Giedion syndrome
-
Verloes A, Moes D, Palumbo L, Elmer C, Francois A, Bricteux G. (1993): Schinzel-Giedion syndrome. Eur J Pediatr (152) 5: 421-423.
-
(1993)
Eur J Pediatr (152)
, vol.5
, pp. 421-423
-
-
Verloes, A.1
Moes, D.2
Palumbo, L.3
Elmer, C.4
Francois, A.5
Bricteux, G.6
|