-
1
-
-
0014772767
-
Metanephric hamartomas and nephroblastomatosis in siblings
-
Liban E, Kozenitzky IL. Metanephric hamartomas and nephroblastomatosis in siblings. Cancer 1970; 25:885-888.
-
(1970)
Cancer
, vol.25
, pp. 885-888
-
-
Liban, E.1
Kozenitzky, I.L.2
-
2
-
-
0015781893
-
Renal hamartomas and nephroblastomatosis with fetal gigantism: A familial syndrome
-
Perlman M, Goldberg GM, Bar-Ziv J, Danovitch G. Renal hamartomas and nephroblastomatosis with fetal gigantism: a familial syndrome. J Pediatr 1973; 83:414-418.
-
(1973)
J Pediatr
, vol.83
, pp. 414-418
-
-
Perlman, M.1
Goldberg, G.M.2
Bar-Ziv, J.3
Danovitch, G.4
-
3
-
-
0016794720
-
Syndrome of fetal gigantism, renal hamartomas, and nephroblastomatosis with Wilms' tumor
-
Perlman M, Levin M, Wittels B. Syndrome of fetal gigantism, renal hamartomas, and nephroblastomatosis with Wilms' tumor. Cancer 1975; 35:1212-1217.
-
(1975)
Cancer
, vol.35
, pp. 1212-1217
-
-
Perlman, M.1
Levin, M.2
Wittels, B.3
-
4
-
-
0023017259
-
Perlman syndrome: Familial renal dysplasia with Wilms tumor, fetal gigantism, and multiple congenital anomalies [letter]
-
Perlman M. Perlman syndrome: familial renal dysplasia with Wilms tumor, fetal gigantism, and multiple congenital anomalies [letter]. Am J Med Genet 1986; 25:793-795.
-
(1986)
Am J Med Genet
, vol.25
, pp. 793-795
-
-
Perlman, M.1
-
5
-
-
0021229493
-
The Perlman syndrome: Familial renal dysplasia with Wilms tumor, fetal gigantism and multiple congenital anomalies
-
Neri G, Martini-Neri ME, Katz BE, Opitz JM. The Perlman syndrome: familial renal dysplasia with Wilms tumor, fetal gigantism and multiple congenital anomalies. Am J Med Genet 1984; 19:195-207.
-
(1984)
Am J Med Genet
, vol.19
, pp. 195-207
-
-
Neri, G.1
Martini-Neri, M.E.2
Katz, B.E.3
Opitz, J.M.4
-
6
-
-
0031891797
-
Perlman syndrome: A case report emphasizing its similarity to and distinction from Beckwith-Wiedemann and prune-belly syndromes
-
Fahmy J, Kaminsky CK, Parisi MT. Perlman syndrome: a case report emphasizing its similarity to and distinction from Beckwith-Wiedemann and prune-belly syndromes. Pediatr Radiol 1998; 28: 179-182.
-
(1998)
Pediatr Radiol
, vol.28
, pp. 179-182
-
-
Fahmy, J.1
Kaminsky, C.K.2
Parisi, M.T.3
-
7
-
-
0031896606
-
Prenatal ultrasound observations in subsequent pregnancies with Perlman syndrome
-
van der Stege JG, van Eyck J, Arabin B. Prenatal ultrasound observations in subsequent pregnancies with Perlman syndrome. Ultrasound Obstet Gynecol 1998; 11:149-151.
-
(1998)
Ultrasound Obstet Gynecol
, vol.11
, pp. 149-151
-
-
Van Der Stege, J.G.1
Van Eyck, J.2
Arabin, B.3
-
8
-
-
0033615472
-
Perlman syndrome: Four additional cases and review
-
Henneveld HT, van Lingen RA, Hamel BC, Stolte-Dijkstra I, van Essen AJ. Perlman syndrome: four additional cases and review. Am J Med Genet 1999; 86:439-446.
-
(1999)
Am J Med Genet
, vol.86
, pp. 439-446
-
-
Henneveld, H.T.1
Van Lingen, R.A.2
Hamel, B.C.3
Stolte-Dijkstra, I.4
Van Essen, A.J.5
-
9
-
-
0031761779
-
Perlman syndrome: A cause of enlarged, hyperechogenic kidneys
-
Chitty LS, Clark T, Maxwell D. Perlman syndrome: a cause of enlarged, hyperechogenic kidneys. Prenat Diagn 1998; 18:1163-1168.
-
(1998)
Prenat Diagn
, vol.18
, pp. 1163-1168
-
-
Chitty, L.S.1
Clark, T.2
Maxwell, D.3
-
10
-
-
0030950727
-
Extending the overlap of three congenital overgrowth syndromes
-
Coppin B, Moore I, Hatchwell E. Extending the overlap of three congenital overgrowth syndromes. Clin Genet 1997; 51:375-378.
-
(1997)
Clin Genet
, vol.51
, pp. 375-378
-
-
Coppin, B.1
Moore, I.2
Hatchwell, E.3
-
11
-
-
0026483207
-
Perlman and Wiedemann-Beckwith syndromes: Two distinct conditions associated with Wilms' tumour
-
Grundy RG, Pritchard J, Baraitser M, Risdon A, Robards M. Perlman and Wiedemann-Beckwith syndromes: two distinct conditions associated with Wilms' tumour. Eur J Pediatr 1992; 151:895-898.
-
(1992)
Eur J Pediatr
, vol.151
, pp. 895-898
-
-
Grundy, R.G.1
Pritchard, J.2
Baraitser, M.3
Risdon, A.4
Robards, M.5
-
12
-
-
0022486675
-
The Perlman familial nephroblastomatosis syndrome
-
Greenberg F, Stein F, Gresik MV, et al. The Perlman familial nephroblastomatosis syndrome. Am J Med Genet 1986; 24:101-110.
-
(1986)
Am J Med Genet
, vol.24
, pp. 101-110
-
-
Greenberg, F.1
Stein, F.2
Gresik, M.V.3
-
13
-
-
0342902019
-
A case of Perlman syndrome associated with a cytogenetic abnormality of chromosome 11
-
Chernos JE, Fowler SB, Cox DM. A case of Perlman syndrome associated with a cytogenetic abnormality of chromosome 11 [abstract]. Am J Hum Genet 1990; 47(suppl):A28.
-
(1990)
Am J Hum Genet
, vol.47
, Issue.SUPPL.
-
-
Chernos, J.E.1
Fowler, S.B.2
Cox, D.M.3
-
14
-
-
0034006094
-
A case of Perlman syndrome: Fetal gigantism, renal dysplasia, and severe neurological deficits
-
Schilke K, Schaefer F, Waldherr R, et al. A case of Perlman syndrome: fetal gigantism, renal dysplasia, and severe neurological deficits. Am J Med Genet 2000; 91:29-33.
-
(2000)
Am J Med Genet
, vol.91
, pp. 29-33
-
-
Schilke, K.1
Schaefer, F.2
Waldherr, R.3
-
15
-
-
0023193362
-
Genetic mechanisms of tumor-specific loss of 11p DNA sequences in Wilms tumor
-
Dao DD, Schroeder WT, Chao LY, et al. Genetic mechanisms of tumor-specific loss of 11p DNA sequences in Wilms tumor. Am J Hum Genet 1987; 41:202-217.
-
(1987)
Am J Hum Genet
, vol.41
, pp. 202-217
-
-
Dao, D.D.1
Schroeder, W.T.2
Chao, L.Y.3
-
16
-
-
0029848437
-
Molecular biology of Beckwith-Wiedemann syndrome
-
Weksberg R, Squire JA. Molecular biology of Beckwith-Wiedemann syndrome. Med Pediatr Oncol 1996; 27:462-469.
-
(1996)
Med Pediatr Oncol
, vol.27
, pp. 462-469
-
-
Weksberg, R.1
Squire, J.A.2
-
17
-
-
0025362975
-
Loss of heterozygosity in Wilms' tumors, studied for 6 putative tumor suppressor regions, is limited to chromosome 11
-
Mannens M, Devilee P, Bliek J, et al. Loss of heterozygosity in Wilms' tumors, studied for 6 putative tumor suppressor regions, is limited to chromosome 11. Cancer Res 1990; 50:3279-3283.
-
(1990)
Cancer Res
, vol.50
, pp. 3279-3283
-
-
Mannens, M.1
Devilee, P.2
Bliek, J.3
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