-
1
-
-
0001031907
-
A child with double cleft of lip and palate, protrusion of the intermaxillary portion of the upper jaw and imperfect development of the bones of the four extremeties
-
Roberts JB. A child with double cleft of lip and palate, protrusion of the intermaxillary portion of the upper jaw and imperfect development of the bones of the four extremeties. Ann Surg 1919: 70: 252-253.
-
(1919)
Ann Surg
, vol.70
, pp. 252-253
-
-
Roberts, J.B.1
-
2
-
-
0016176846
-
The Roberts syndrome
-
Freeman MV, Williams DW, Schimke RN, Temtamy SA, Vachier E, German J. The Roberts syndrome. Clin Genet 1974: 5: 1-16.
-
(1974)
Clin Genet
, vol.5
, pp. 1-16
-
-
Freeman, M.V.1
Williams, D.W.2
Schimke, R.N.3
Temtamy, S.A.4
Vachier, E.5
German, J.6
-
3
-
-
0027429318
-
Roberts syndrome: A review of 100 cases and a new rating system for severity
-
Van Den Berg DJ, Francke U. Roberts syndrome: a review of 100 cases and a new rating system for severity. Am J Med Genet 1993: 47: 1104-1123.
-
(1993)
Am J Med Genet
, vol.47
, pp. 1104-1123
-
-
Van Den Berg, D.J.1
Francke, U.2
-
5
-
-
0024318646
-
Prenatal detection of Roberts-SC phocomelia syndrome: Report of two sibs with characteristic manifestations
-
Robins DB, Ladda RL, Thieme GA, Boal DK, Emanuel BS, Zackai EH. Prenatal detection of Roberts-SC phocomelia syndrome: report of two sibs with characteristic manifestations. Am J Med Genet 1989: 32: 390-394.
-
(1989)
Am J Med Genet
, vol.32
, pp. 390-394
-
-
Robins, D.B.1
Ladda, R.L.2
Thieme, G.A.3
Boal, D.K.4
Emanuel, B.S.5
Zackai, E.H.6
-
6
-
-
0025035631
-
A sibship with Roberts/SC phocomelia syndrome
-
Holmes-Siedle M, Seres-Santamaria A, Crocker M, Hall JG, Crouchman M. A sibship with Roberts/SC phocomelia syndrome. Am J Med Genet 1990: 37: 18-22.
-
(1990)
Am J Med Genet
, vol.37
, pp. 18-22
-
-
Holmes-Siedle, M.1
Seres-Santamaria, A.2
Crocker, M.3
Hall, J.G.4
Crouchman, M.5
-
7
-
-
0002420827
-
A familiar dysmorphogenetic syndrome of limb deformities, characteristic facial appearance and associated anomalies: The 'pseudothalidomide' or 'SC-syndrome'
-
Bergsma D, McKusick V, Hall J, Scott C, eds. New York: Alan R Liss, for the National Foundation - March of Dimes. BD:OAS
-
Herrmann J, Feingold M, Tuffli GA, Opitz JM. A familiar dysmorphogenetic syndrome of limb deformities, characteristic facial appearance and associated anomalies: the 'pseudothalidomide' or 'SC-syndrome'. In: Bergsma D, McKusick V, Hall J, Scott C, eds. The Clinical Delineation of Birth Defects: Part III, Limb Malformations. New York: Alan R Liss, for the National Foundation - March of Dimes. BD:OAS, 1969: 5(3): 81-89.
-
(1969)
The Clinical Delineation of Birth Defects: Part III, Limb Malformations
, vol.5
, Issue.3
, pp. 81-89
-
-
Herrmann, J.1
Feingold, M.2
Tuffli, G.A.3
Opitz, J.M.4
-
8
-
-
0023154710
-
Roberts syndrome and SC phocomelia. A single genetic entity
-
Romke C, Froster-Iskenius U, Heyne K, Hohn W, Hof M, Grzejszyk G, Rauskolb R, Rehder H, Schwinger E. Roberts syndrome and SC phocomelia. A single genetic entity. Clin Genet 1987: 31: 170-177.
-
(1987)
Clin Genet
, vol.31
, pp. 170-177
-
-
Romke, C.1
Froster-Iskenius, U.2
Heyne, K.3
Hohn, W.4
Hof, M.5
Grzejszyk, G.6
Rauskolb, R.7
Rehder, H.8
Schwinger, E.9
-
9
-
-
0022510457
-
SC phocomelia syndrome, premature centromere separation, and congenital cranial nerve paralysis in two sisters, one with malignant melanoma
-
Parry DM, Mulvihill JJ, Tsai S, Kaiser-Kupfer M, Cowan JM. SC phocomelia syndrome, premature centromere separation, and congenital cranial nerve paralysis in two sisters, one with malignant melanoma. Am J Med Genet 1986: 24: 653-672.
-
(1986)
Am J Med Genet
, vol.24
, pp. 653-672
-
-
Parry, D.M.1
Mulvihill, J.J.2
Tsai, S.3
Kaiser-Kupfer, M.4
Cowan, J.M.5
-
10
-
-
0025289046
-
The Baller-Gerold syndrome: Phenotypic and cytogenetic overlap with Roberts syndrome
-
Huson SM, Rodgers CS, Hall CM, Winter RM. The Baller-Gerold syndrome: phenotypic and cytogenetic overlap with Roberts syndrome. J Med Genet 1990: 27: 371-375.
-
(1990)
J Med Genet
, vol.27
, pp. 371-375
-
-
Huson, S.M.1
Rodgers, C.S.2
Hall, C.M.3
Winter, R.M.4
-
11
-
-
0021677553
-
Abnormalities in the cell-division cycle in Roberts syndrome fibroblasts: A cellular basis for the phenotypic characteristics?
-
Tomkins DJ, Sisken JE. Abnormalities in the cell-division cycle in Roberts syndrome fibroblasts: a cellular basis for the phenotypic characteristics? Am J Hum Genet 1984: 36: 1332-1340.
-
(1984)
Am J Hum Genet
, vol.36
, pp. 1332-1340
-
-
Tomkins, D.J.1
Sisken, J.E.2
-
12
-
-
0025772088
-
Studies of the mitotic and centromeric abnormalities in Roberts syndrome: Implications for a defect in the mitotic mechanism
-
Jabs EW, Tuck-Muller C, Cusano R, Rattner JB. Studies of the mitotic and centromeric abnormalities in Roberts syndrome: implications for a defect in the mitotic mechanism. Chromosoma 1991: 100: 251-261.
-
(1991)
Chromosoma
, vol.100
, pp. 251-261
-
-
Jabs, E.W.1
Tuck-Muller, C.2
Cusano, R.3
Rattner, J.B.4
-
13
-
-
26444577275
-
Eine seltene menschliche Missbildung und ihre Bedeutung fur die Entwicklungsgeschichte
-
Falk E. Eine seltene menschliche Missbildung und ihre Bedeutung fur die Entwicklungsgeschichte. Virchows Arch Path Anat 1908: 192: 544-564.
-
(1908)
Virchows Arch Path Anat
, vol.192
, pp. 544-564
-
-
Falk, E.1
-
14
-
-
0026352896
-
Roberts syndrome: Phenotypic variation, cytogenetic definition and heterozygote detection
-
Maserati E, Pasquali F, Zuffardi O, Buttitta P, Cuoco C, Defant G, Gimelli G, Fraccaro M. Roberts syndrome: phenotypic variation, cytogenetic definition and heterozygote detection. Ann Genet 1991: 34: 239-246.
-
(1991)
Ann Genet
, vol.34
, pp. 239-246
-
-
Maserati, E.1
Pasquali, F.2
Zuffardi, O.3
Buttitta, P.4
Cuoco, C.5
Defant, G.6
Gimelli, G.7
Fraccaro, M.8
-
15
-
-
0024459338
-
Roberts-SC phocomelia syndrome with exencephaly
-
Verloes A, Herens C, Van ML, Retz MC, Dodinval P. Roberts-SC phocomelia syndrome with exencephaly. Ann Genet 1989: 32: 169-170.
-
(1989)
Ann Genet
, vol.32
, pp. 169-170
-
-
Verloes, A.1
Herens, C.2
Van, M.L.3
Retz, M.C.4
Dodinval, P.5
-
16
-
-
4243296913
-
Morphological evidence of disturbed chromosome separation in Roberts syndrome: A human mitotic mutant
-
Louie E, German J. Morphological evidence of disturbed chromosome separation in Roberts syndrome: a human mitotic mutant. J Cell Biol 1983: 97: 192A.
-
(1983)
J Cell Biol
, vol.97
-
-
Louie, E.1
German, J.2
-
17
-
-
0031759278
-
Expression of apoptotic and proliferation markers in meningiomas
-
In Press
-
Konstantinidou AE, Pavlopoulos PM, Patsouris E, Kaklamanis L, Davaris P. (1998): Expression of apoptotic and proliferation markers in meningiomas. J Pathol, In Press.
-
(1998)
J Pathol
-
-
Konstantinidou, A.E.1
Pavlopoulos, P.M.2
Patsouris, E.3
Kaklamanis, L.4
Davaris, P.5
-
18
-
-
0018595224
-
Roberts' syndrome. I. Cytological evidence for a disturbance in chromatid pairing
-
German J. Roberts' syndrome. I. Cytological evidence for a disturbance in chromatid pairing. Clin Genet 1979: 16: 441-447.
-
(1979)
Clin Genet
, vol.16
, pp. 441-447
-
-
German, J.1
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