-
1
-
-
0015831045
-
A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular, and limb anomalies
-
Cohen MM Jr, Hall BD, Smith DW, Graham CB, Lampert KJ. A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular, and limb anomalies. J Pediatr 1973;83:280-4.
-
(1973)
J Pediatr
, vol.83
, pp. 280-284
-
-
Cohen M.M., Jr.1
Hall, B.D.2
Smith, D.W.3
Graham, C.B.4
Lampert, K.J.5
-
2
-
-
0017882399
-
Confirmation of the Cohen syndrome
-
Carey JC, Hall BD. Confirmation of the Cohen syndrome. J Pediatr 1978;93:239-44.
-
(1978)
J Pediatr
, vol.93
, pp. 239-244
-
-
Carey, J.C.1
Hall, B.D.2
-
4
-
-
0025808573
-
Síndrome de Cohen: Presentación de dos casos de gemelas
-
Arcas Martinez J, García Penas JJ, Ramos Lizana J, Díaz Gonzalez C, Pascual Castroviejo I. Síndrome de Cohen: presentación de dos casos de gemelas. An Esp Pediatr 1991;34:83-5.
-
(1991)
An Esp Pediatr
, vol.34
, pp. 83-85
-
-
Arcas Martinez, J.1
García Penas, J.J.2
Ramos Lizana, J.3
Díaz Gonzalez, C.4
Pascual Castroviejo, I.5
-
5
-
-
0031440471
-
A familiar syndrome with hypotonia, mental retardation and dysmorphic features resembling Cohen syndrome
-
Mejia-Baltodano G, Bobadilla L, Solís A, Mendoza R, Díaz-Gallardo MY, Barros-Nunez P. A familiar syndrome with hypotonia, mental retardation and dysmorphic features resembling Cohen syndrome. Genet Couns 1997;8:311-6.
-
(1997)
Genet Couns
, vol.8
, pp. 311-316
-
-
Mejia-Baltodano, G.1
Bobadilla, L.2
Solís, A.3
Mendoza, R.4
Díaz-Gallardo, M.Y.5
Barros-Nunez, P.6
-
6
-
-
0028305381
-
Cohen syndrome gene assigned to the long arm of chromosome 8 by linkage analysis
-
Tahvanainen E, Norio R, Karila E, Ranta S, Weissenbach J, Sistonen P, et al. Cohen syndrome gene assigned to the long arm of chromosome 8 by linkage analysis. Nat Genet 1994;7:201-4.
-
(1994)
Nat Genet
, vol.7
, pp. 201-204
-
-
Tahvanainen, E.1
Norio, R.2
Karila, E.3
Ranta, S.4
Weissenbach, J.5
Sistonen, P.6
-
7
-
-
0035862567
-
An integrated physical map of 8q22-q24: Use in positional cloning and deletion analysis of Langer-Giedion syndrome
-
Hilton MJ, Gutierrez L, Zhang L, Moreno PA, Reddy M, Brown N, et al. An integrated physical map of 8q22-q24: use in positional cloning and deletion analysis of Langer-Giedion syndrome. Genomics 2001;71:192-9.
-
(2001)
Genomics
, vol.71
, pp. 192-199
-
-
Hilton, M.J.1
Gutierrez, L.2
Zhang, L.3
Moreno, P.A.4
Reddy, M.5
Brown, N.6
-
8
-
-
0021360153
-
Further delineation of the Cohen syndrome; report on chorioretinal dystrophy, leukopenia and consanguinity
-
Norio R, Raitta C, Lindahl E. Further delineation of the Cohen syndrome; report on chorioretinal dystrophy, leukopenia and consanguinity. Clin Genet 1984;25:1-14.
-
(1984)
Clin Genet
, vol.25
, pp. 1-14
-
-
Norio, R.1
Raitta, C.2
Lindahl, E.3
-
9
-
-
0020263375
-
The Cohen syndrome: Report of five new cases and a review of the literature
-
Friedman E, Sack J. The Cohen syndrome: report of five new cases and a review of the literature. J Craniofac Genet Dev Biol 1982;2:193-200.
-
(1982)
J Craniofac Genet Dev Biol
, vol.2
, pp. 193-200
-
-
Friedman, E.1
Sack, J.2
-
10
-
-
0031131692
-
Periodontal findings in Cohen syndrome with chronic neutropenia
-
Alaluusua S, Kivitie-Kallio S, Wolf J, Haavio ML, Asikainen S, Pirinen S. Periodontal findings in Cohen syndrome with chronic neutropenia. J Periodontol 1997;68:473-8.
-
(1997)
J Periodontol
, vol.68
, pp. 473-478
-
-
Alaluusua, S.1
Kivitie-Kallio, S.2
Wolf, J.3
Haavio, M.L.4
Asikainen, S.5
Pirinen, S.6
-
11
-
-
0032153404
-
Cohen syndrome with neutropenia-induced periodontitis managed with granulocyte colony-stimulating factor (G-CSF): Case reports
-
Seow WK, Bartold PM, Thong YH, Taylor K. Cohen syndrome with neutropenia-induced periodontitis managed with granulocyte colony-stimulating factor (G-CSF): case reports. Pediatr Dent 1998;20:350-4.
-
(1998)
Pediatr Dent
, vol.20
, pp. 350-354
-
-
Seow, W.K.1
Bartold, P.M.2
Thong, Y.H.3
Taylor, K.4
-
14
-
-
0027987990
-
Cohen syndrome is neither uncommon nor new
-
Norio R. Cohen syndrome is neither uncommon nor new. Am J Med Genet 1994;53:202-3.
-
(1994)
Am J Med Genet
, vol.53
, pp. 202-203
-
-
Norio, R.1
-
15
-
-
0029980251
-
Cohen syndrome: The clinical symptoms and stigmata at a young age
-
Fryns JP, Legius E, Devriendt K, Meire F, Standaert L, Baten E, et al. Cohen syndrome: the clinical symptoms and stigmata at a young age. Clin Genet 1996;49:237-41.
-
(1996)
Clin Genet
, vol.49
, pp. 237-241
-
-
Fryns, J.P.1
Legius, E.2
Devriendt, K.3
Meire, F.4
Standaert, L.5
Baten, E.6
-
16
-
-
85031139517
-
Study of mesiodistal diameters in permanent dentition in Spanish child population
-
Marin Ferrer JM, Barbería Leache E, Moreno Gonzĺez JP, Planells del Pozo P, de Nova García J, Costa Ferrer F. Study of mesiodistal diameters in permanent dentition in Spanish child population. Odontol Pediatr 1993;2:67-76.
-
(1993)
Odontol Pediatr
, vol.2
, pp. 67-76
-
-
Marin Ferrer, J.M.1
Barbería Leache, E.2
Moreno Gonzĺez, J.P.3
Planells Del Pozo, P.4
De Nova García, J.5
Costa Ferrer, F.6
-
19
-
-
0029265567
-
Sindrome di Cohen: Un nuova caso e revisione della letteratura
-
Calzolari S, Ballardini M, De Marco P. Sindrome di Cohen. Un nuova caso e revisione della letteratura. Minerva Pediatr 1995;47:83-7.
-
(1995)
Minerva Pediatr
, vol.47
, pp. 83-87
-
-
Calzolari, S.1
Ballardini, M.2
De Marco, P.3
|