-
1
-
-
0003754609
-
Extreme cytomegaly of the adrenal fetal cortex, omphalocele, hyperplasia of the kidneys and pancreas and leydig cell hyperplasia-another syndrome?
-
California, November 11
-
Beckwith JB. Extreme cytomegaly of the adrenal fetal cortex, omphalocele, hyperplasia of the kidneys and pancreas and leydig cell hyperplasia-another syndrome? Presented at the Annual Meeting of Western Society for Pediatric Research Los Angeles, California, November 11, 1963.
-
(1963)
Annual Meeting of Western Society for Pediatric Research Los Angeles
-
-
Beckwith, J.B.1
-
2
-
-
76549164702
-
Complexe malformatif familial avec hernie ombilicale et macroglossie "unsyndrome noveau?"
-
Wiedemann HR. Complexe malformatif familial avec hernie ombilicale et macroglossie "unsyndrome noveau?" J Genet Hum 1964; 13: 223-232.
-
(1964)
J Genet Hum
, vol.13
, pp. 223-232
-
-
Wiedemann, H.R.1
-
4
-
-
34250134720
-
Tumors and hemihypertrophy associated with Wiedemann-Beckwith syndrome
-
Wiedmann HR. Tumors and hemihypertrophy associated with Wiedemann-Beckwith syndrome. Eur J Pediatr 1983; 145: 129-135.
-
(1983)
Eur J Pediatr
, vol.145
, pp. 129-135
-
-
Wiedmann, H.R.1
-
6
-
-
0031940675
-
Risk of cancer during the first four years of life in children from the Beckwith-Wiedemann syndrome registry
-
De Baun MR, Tucker MA. Risk of cancer during the first four years of life in children from the Beckwith-Wiedemann syndrome registry. J Pediatr 1998; 132: 398-400.
-
(1998)
J Pediatr
, vol.132
, pp. 398-400
-
-
De Baun, M.R.1
Tucker, M.A.2
-
7
-
-
0018835921
-
Complete and incomplete forms of Beckwith-Wiedemann syndrome: Their oncogenic potential
-
Sotelo-Avila C, Gonzalez-crussi F, Fowler JW. Complete and incomplete forms of Beckwith-Wiedemann syndrome: Their oncogenic potential. J Pediatr 1980; 96: 47-50.
-
(1980)
J Pediatr
, vol.96
, pp. 47-50
-
-
Sotelo-Avila, C.1
Gonzalez-crussi, F.2
Fowler, J.W.3
-
8
-
-
0029160420
-
Favorable outcome in children with Beckwith-Wiedemann Syndrome and intra abdominal tumors
-
Glazevughan W, Sanders DW, Grosfeld JL Plumley DA, Rescoria FJ, Scherer III L, et al. Favorable outcome in children with Beckwith-Wiedemann Syndrome and intra abdominal tumors. J Pediatr Surg 1995; 30: 1042-1045.
-
(1995)
J Pediatr Surg
, vol.30
, pp. 1042-1045
-
-
Glazevughan, W.1
Sanders, D.W.2
Grosfeld, J.L.3
Plumley, D.A.4
Rescoria, F.J.5
Scherer III, L.6
-
9
-
-
0032711844
-
Congenital hepatoblastoma and schizencephaly in an infant with Beckwith-Wiedemann syndrome
-
Laura LW, Slopis JM, Herzog CE. Congenital hepatoblastoma and schizencephaly in an infant with Beckwith-Wiedemann syndrome. Med Ped Oncol 1999; 33: 591-593.
-
(1999)
Med Ped Oncol
, vol.33
, pp. 591-593
-
-
Laura, L.W.1
Slopis, J.M.2
Herzog, C.E.3
-
10
-
-
0030817649
-
Congenital mesoblalstic nephroma in a child with Beckwith-Wiedemann syndrome
-
Sutherland RW, Wiener JS, Hicks MJ, Hawkins EP, Chintagampala M. Congenital mesoblalstic nephroma in a child with Beckwith-Wiedemann syndrome. J Urol 1997; 158: 1532-1533.
-
(1997)
J Urol
, vol.158
, pp. 1532-1533
-
-
Sutherland, R.W.1
Wiener, J.S.2
Hicks, M.J.3
Hawkins, E.P.4
Chintagampala, M.5
-
11
-
-
0016906657
-
Neoplasms associated with Beckwith-Wiedermann syndrome
-
Sotelo-Avila C, Gooch WM. Neoplasms associated with Beckwith-Wiedermann syndrome. Perspect Pediatr Pathol 1976; 3: 255-272.
-
(1976)
Perspect Pediatr Pathol
, vol.3
, pp. 255-272
-
-
Sotelo-Avila, C.1
Gooch, W.M.2
-
12
-
-
0022918905
-
Constitutional interstitial deletion of 11p11 and pericentric inversion of chromosome 9 in a patient with Wiedemann-Beckwith syndrome and hepatoblastoma
-
Haas OA, Zoubek A, Grumayer ER, Gadner H. Constitutional interstitial deletion of 11p11 and pericentric inversion of chromosome 9 in a patient with Wiedemann-Beckwith syndrome and hepatoblastoma. Cancer Genet Cytogent 1986; 23: 95-104.
-
(1986)
Cancer Genet Cytogent
, vol.23
, pp. 95-104
-
-
Haas, O.A.1
Zoubek, A.2
Grumayer, E.R.3
Gadner, H.4
-
14
-
-
0028000817
-
Molecular analysis of a patient with Beckwith-Wiedemann syndrome, Rhabdomyosarcoma and renal cell carcinoma
-
Matsumoto T, Kinoshita E, Maeda H, Nikawa N, Kurosaki N, Harada N, et al. Molecular analysis of a patient with Beckwith-Wiedemann syndrome, Rhabdomyosarcoma and renal cell carcinoma. Japan J Hum Genet 1994; 39: 225-234.
-
(1994)
Japan J Hum Genet
, vol.39
, pp. 225-234
-
-
Matsumoto, T.1
Kinoshita, E.2
Maeda, H.3
Nikawa, N.4
Kurosaki, N.5
Harada, N.6
-
15
-
-
0032086841
-
Urinary bladder rhabdomyosarcoma associated with Beckwith-Wiedemann syndrome
-
Aideyan LO, Kao SCS. Urinary bladder rhabdomyosarcoma associated with Beckwith-Wiedemann syndrome. Clin Radiol 1998; 53: 457-459.
-
(1998)
Clin Radiol
, vol.53
, pp. 457-459
-
-
Aideyan, L.O.1
Kao, S.C.S.2
-
16
-
-
0032959785
-
Hemihypertrophy and a poorly differentiated embryonal rhabdomyosarcoma of the pelvis
-
Samuel DP, Tsokos M, DeBaun MR. Hemihypertrophy and a poorly differentiated embryonal rhabdomyosarcoma of the pelvis. Med Pediatr Oncol 1999; 32: 38-43.
-
(1999)
Med Pediatr Oncol
, vol.32
, pp. 38-43
-
-
Samuel, D.P.1
Tsokos, M.2
DeBaun, M.R.3
-
17
-
-
0015508247
-
The Wiedemann-Beckwith syndrome: Genetic consideration and a diagnostic sign
-
Kosseff AI, Hermann J, Optiz JM. The Wiedemann-Beckwith syndrome: Genetic consideration and a diagnostic sign. Lancet 1872; 1: 844.
-
(1872)
Lancet
, vol.1
, pp. 844
-
-
Kosseff, A.I.1
Hermann, J.2
Optiz, J.M.3
-
18
-
-
0022910322
-
Wiedemann-Beckwith syndrome. Presentation of clinical and cytogenetic data of 22 new cases and review of literature
-
Petgtenati MJ, Haines JL, Higgins RR, Wappner RS, Palmer CG, Weaver DD. Wiedemann-Beckwith syndrome. Presentation of clinical and cytogenetic data of 22 new cases and review of literature. Hum Genet 1986; 74: 143-154.
-
(1986)
Hum Genet
, vol.74
, pp. 143-154
-
-
Petgtenati, M.J.1
Haines, J.L.2
Higgins, R.R.3
Wappner, R.S.4
Palmer, C.G.5
Weaver, D.D.6
-
19
-
-
0023033292
-
Macroglossia: A review of the condition and a new classification
-
Vogel JE, Mulliken JB, Kaban LB. Macroglossia: A review of the condition and a new classification. Plast Reconstr Surg 1986; 78: 715-723.
-
(1986)
Plast Reconstr Surg
, vol.78
, pp. 715-723
-
-
Vogel, J.E.1
Mulliken, J.B.2
Kaban, L.B.3
-
20
-
-
0023832163
-
Congenital anomalies associated with RMS: An autopsy study of 115 cases. A report from the intergroup rhabdomyosarcoma study committee (representing the Children Cancer Study Group, the Pediatrics Oncology Group, the United Kingdom Children Cancer Study Group and the Pediatrics Intergroup Statistical Center)
-
Ruymann FB, Maddux HR, Ragab A, Soule EH, Palmer N, Beltangady M et al. Congenital anomalies associated with RMS: An autopsy study of 115 cases. A report from the intergroup rhabdomyosarcoma study committee (representing the Children Cancer Study Group, the Pediatrics Oncology Group, the United Kingdom Children Cancer Study Group and the Pediatrics Intergroup Statistical Center). Med Pediatr Oncol 1988; 16: 33-39.
-
(1988)
Med Pediatr Oncol
, vol.16
, pp. 33-39
-
-
Ruymann, F.B.1
Maddux, H.R.2
Ragab, A.3
Soule, E.H.4
Palmer, N.5
Beltangady, M.6
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