-
1
-
-
0019787622
-
Congenital hypertrophic pyloric stenosis and associated anomalies in the genitourinary tract
-
Atwell JD, Levick P (1981) Congenital hypertrophic pyloric stenosis and associated anomalies in the genitourinary tract. J Pediatr Surg 16:1029-1035
-
(1981)
J Pediatr Surg
, vol.16
, pp. 1029-1035
-
-
Atwell, J.D.1
Levick, P.2
-
2
-
-
0023156312
-
Measuring birth defects and handicapping disorders in the population: The British Columbia Health Surveillance Registry
-
Baird PA (1987) Measuring birth defects and handicapping disorders in the population: the British Columbia Health Surveillance Registry. Can Med Assoc J 36:109-111
-
(1987)
Can Med Assoc J
, vol.36
, pp. 109-111
-
-
Baird, P.A.1
-
3
-
-
0024592746
-
Neurofibromatosis and other disorders among children with CNS tumors and their families
-
Baptiste M, Nasca P, Metzger B, Field N, McCubbi P, Greenwald P, Armbrustmacher V, et al (1989) Neurofibromatosis and other disorders among children with CNS tumors and their families. Neurology 39:487-492
-
(1989)
Neurology
, vol.39
, pp. 487-492
-
-
Baptiste, M.1
Nasca, P.2
Metzger, B.3
Field, N.4
McCubbi, P.5
Greenwald, P.6
Armbrustmacher, V.7
-
4
-
-
0027534945
-
Rearrangement of the PAX3 paired box gene in the paediatric solid tumour alveolar rhabdomyosarcoma
-
Barr FG, Galili N, Holick J, Biegel JA, Rovera G, Emanuel BS (1993) Rearrangement of the PAX3 paired box gene in the paediatric solid tumour alveolar rhabdomyosarcoma. Nat Genet 3:113-117
-
(1993)
Nat Genet
, vol.3
, pp. 113-117
-
-
Barr, F.G.1
Galili, N.2
Holick, J.3
Biegel, J.A.4
Rovera, G.5
Emanuel, B.S.6
-
5
-
-
0014769537
-
Coincidence of congenital malformation and embryonic tumors of childhood
-
Berry CL, Keeling J, Hilton C (1970) Coincidence of congenital malformation and embryonic tumors of childhood. Arch Dis Child 45:229-231
-
(1970)
Arch Dis Child
, vol.45
, pp. 229-231
-
-
Berry, C.L.1
Keeling, J.2
Hilton, C.3
-
6
-
-
0023473455
-
A classification scheme for childhood cancer
-
Birch JM, Marsden HB (1987) A classification scheme for childhood cancer. Int J Cancer 40:620-624
-
(1987)
Int J Cancer
, vol.40
, pp. 620-624
-
-
Birch, J.M.1
Marsden, H.B.2
-
7
-
-
0020035010
-
Prenatal factors in the origin of germ cell tumors in childhood
-
Birch JM, Marsden HB, Swindell R (1982) Prenatal factors in the origin of germ cell tumors in childhood. Carcinogenesis 3:75-80
-
(1982)
Carcinogenesis
, vol.3
, pp. 75-80
-
-
Birch, J.M.1
Marsden, H.B.2
Swindell, R.3
-
9
-
-
0026704427
-
Genetics and genetic epidemiology of Wilms' tumour in the French Wilms' Tumour Study
-
Bonaiti-Pellie C, Chompret A, Tournade M-F, Hochez J, Moutou C, Zucker J-M, Steschenko D, et al (1992) Genetics and genetic epidemiology of Wilms' tumour in the French Wilms' Tumour Study. Med Pediatr Oncol 20:284-291
-
(1992)
Med Pediatr Oncol
, vol.20
, pp. 284-291
-
-
Bonaiti-Pellie, C.1
Chompret, A.2
Tournade, M.-F.3
Hochez, J.4
Moutou, C.5
Zucker, J.-M.6
Steschenko, D.7
-
10
-
-
0027205493
-
Relation between maternal diet and subsequent primitive neuroectodermal brain tumors in young children
-
Bunin GR, Kuitjen RR, Buckley JD, Rorke LB, Meadows AT (1993) Relation between maternal diet and subsequent primitive neuroectodermal brain tumors in young children. N Engl J Med 329:536-541
-
(1993)
N Engl J Med
, vol.329
, pp. 536-541
-
-
Bunin, G.R.1
Kuitjen, R.R.2
Buckley, J.D.3
Rorke, L.B.4
Meadows, A.T.5
-
11
-
-
0027465535
-
Genetic mosaicism in normal tissue of Wilms tumour patients
-
Chao L-Y, Huff V, Tomlinson G, Riccardi VM, Strong LC, Saunders GF (1993) Genetic mosaicism in normal tissue of Wilms tumour patients. Nat Genet 3:127-131
-
(1993)
Nat Genet
, vol.3
, pp. 127-131
-
-
Chao, L.-Y.1
Huff, V.2
Tomlinson, G.3
Riccardi, V.M.4
Strong, L.C.5
Saunders, G.F.6
-
12
-
-
16944366387
-
Autosomal dominant inheritance of Wilms tumor and branchial cleft anomalies: A new syndrome?
-
Cich JA (1993) Autosomal dominant inheritance of Wilms tumor and branchial cleft anomalies: a new syndrome? Causes Childhood Cancer Newslett 4(2): 1-2
-
(1993)
Causes Childhood Cancer Newslett
, vol.4
, Issue.2
, pp. 1-2
-
-
Cich, J.A.1
-
13
-
-
0027325341
-
Congenital anomalies and genetic syndromes in 173 cases of medulloblastoma
-
Evans G, Burnell L, Campbell R, Gattamaneni HR, Birch J (1993) Congenital anomalies and genetic syndromes in 173 cases of medulloblastoma Med Pediatr Oncol 21:433-434
-
(1993)
Med Pediatr Oncol
, vol.21
, pp. 433-434
-
-
Evans, G.1
Burnell, L.2
Campbell, R.3
Gattamaneni, H.R.4
Birch, J.5
-
15
-
-
0015225140
-
Adenocarcinoma of the vagina: Association of maternal stilbestrol therapy with tumor appearance in young women
-
Herbst AL, Cole P, Carlton T, Robbay ST, Scully RE (1971) Adenocarcinoma of the vagina: association of maternal stilbestrol therapy with tumor appearance in young women. N Engl J Med 284;878-881
-
(1971)
N Engl J Med
, vol.284
, pp. 878-881
-
-
Herbst, A.L.1
Cole, P.2
Carlton, T.3
Robbay, S.T.4
Scully, R.E.5
-
16
-
-
0014084624
-
Osteosarcoma occurring in osteogenesis imperfecta: Report of two cases
-
Klenerman L, Ockenden BG, Townsend AC (1967) Osteosarcoma occurring in osteogenesis imperfecta: report of two cases. J Bone Joint Surg 49:314-323
-
(1967)
J Bone Joint Surg
, vol.49
, pp. 314-323
-
-
Klenerman, L.1
Ockenden, B.G.2
Townsend, A.C.3
-
17
-
-
0014296440
-
Wilms' tumor and congenital heart disease: Report of a case and a family
-
Lynch HT, Green GS (1968) Wilms' tumor and congenital heart disease: report of a case and a family. Am J Dis Child 115:723-726
-
(1968)
Am J Dis Child
, vol.115
, pp. 723-726
-
-
Lynch, H.T.1
Green, G.S.2
-
18
-
-
0027220557
-
Congenital abnormalities in children with cancer and their relatives: Results from a case-control study (IRESCC)
-
Mann JR, Dodd HE, Draper GJ, Waterhouse JAH, Birch JM, Cartwright RA, Hartley AL, et al (1993) Congenital abnormalities in children with cancer and their relatives: results from a case-control study (IRESCC). Br J Cancer 357-363
-
(1993)
Br J Cancer
, pp. 357-363
-
-
Mann, J.R.1
Dodd, H.E.2
Draper, G.J.3
Waterhouse, J.A.H.4
Birch, J.M.5
Cartwright, R.A.6
Hartley, A.L.7
-
19
-
-
0025028214
-
Malignant hepatic tumors in children: Incidence, clinical features and etiology
-
Mann JR, Kasthuri N, Raafat F, Pincott JR, Parkes SE, Muir KR, Ingram LC, et al (1990) Malignant hepatic tumors in children: incidence, clinical features and etiology. Paediatr Perinat Epidemiol 4:276-289
-
(1990)
Paediatr Perinat Epidemiol
, vol.4
, pp. 276-289
-
-
Mann, J.R.1
Kasthuri, N.2
Raafat, F.3
Pincott, J.R.4
Parkes, S.E.5
Muir, K.R.6
Ingram, L.C.7
-
21
-
-
0021815955
-
Increased prevalence of minor anomalies in childhood malignancy
-
Mehes K, Signer E, Pluss HJ, Muller HJ, Stalder G (1985) Increased prevalence of minor anomalies in childhood malignancy. Eur J Pediatr 144:243-249
-
(1985)
Eur J Pediatr
, vol.144
, pp. 243-249
-
-
Mehes, K.1
Signer, E.2
Pluss, H.J.3
Muller, H.J.4
Stalder, G.5
-
22
-
-
0027502746
-
Risk of childhood cancer for infants with birth defects. I. A record linkage study, Atlanta, Georgia 1968-1988
-
Mili F, Khoury MJ, Flanders WD, Greenberg RS (1993A) Risk of childhood cancer for infants with birth defects. I. A record linkage study, Atlanta, Georgia 1968-1988. Am J Epidemiol 137:629-638
-
(1993)
Am J Epidemiol
, vol.137
, pp. 629-638
-
-
Mili, F.1
Khoury, M.J.2
Flanders, W.D.3
Greenberg, R.S.4
-
23
-
-
0001073142
-
Down's syndrome (mongolism), other congenital malformations and cancers among the sibs of leukemic children
-
Miller RW (1963) Down's syndrome (mongolism), other congenital malformations and cancers among the sibs of leukemic children. N Engl J Med 268:393-401
-
(1963)
N Engl J Med
, vol.268
, pp. 393-401
-
-
Miller, R.W.1
-
24
-
-
0014287354
-
Relation between cancer and congenital defects: And epidemiologic evaluation
-
_ (1968) Relation between cancer and congenital defects: and epidemiologic evaluation. J Natl Cancer Inst 40:1079-1085
-
(1968)
J Natl Cancer Inst
, vol.40
, pp. 1079-1085
-
-
-
25
-
-
78651152965
-
Association of Wilms' tumour with aniridia, hemihypertrophy and other congenital abnormalities
-
Miller RW, Fraumeni JF, Manning MD (1964) Association of Wilms' tumour with aniridia, hemihypertrophy and other congenital abnormalities. N Engl J Med 207:922-927
-
(1964)
N Engl J Med
, vol.207
, pp. 922-927
-
-
Miller, R.W.1
Fraumeni, J.F.2
Manning, M.D.3
-
27
-
-
0030002141
-
The molecular basis of hypodactyly (Hd): A deletion in HOXa13 leads to arrest of digital arch formation
-
Mortlock DP, Post LC, Innis JW (1996) The molecular basis of hypodactyly (Hd): a deletion in HOXa13 leads to arrest of digital arch formation. Nat Genet 13:284-289
-
(1996)
Nat Genet
, vol.13
, pp. 284-289
-
-
Mortlock, D.P.1
Post, L.C.2
Innis, J.W.3
-
28
-
-
0020627270
-
A recognizable pattern of the midface of retinoblastoma patients with interstitial deletion of 13q
-
Motegi T, Kaga M, Yanagawa Y, Kadowaki H, Watanabe K, Inove A, Komatsu M, et al (1983) A recognizable pattern of the midface of retinoblastoma patients with interstitial deletion of 13q. Hum Genet 64:160-162
-
(1983)
Hum Genet
, vol.64
, pp. 160-162
-
-
Motegi, T.1
Kaga, M.2
Yanagawa, Y.3
Kadowaki, H.4
Watanabe, K.5
Inove, A.6
Komatsu, M.7
-
29
-
-
0023791890
-
Periconceptual use of multivitamins and the occurrence of neural tube defects
-
Mulinare J, Cordero JF, Erickson JD, Berry RJ (1988) Periconceptual use of multivitamins and the occurrence of neural tube defects. JAMA 260:3141-3145
-
(1988)
JAMA
, vol.260
, pp. 3141-3145
-
-
Mulinare, J.1
Cordero, J.F.2
Erickson, J.D.3
Berry, R.J.4
-
30
-
-
0017679043
-
Multiple childhood osteosarcomas in an American Indian family with erythroid macrocytosis and skeletal anomalies
-
Mulvihill JJ, Gralnick HR, Whang-Peng J, Leventhal BG (1977) Multiple childhood osteosarcomas in an American Indian family with erythroid macrocytosis and skeletal anomalies. Cancer 40:3115-3122
-
(1977)
Cancer
, vol.40
, pp. 3115-3122
-
-
Mulvihill, J.J.1
Gralnick, H.R.2
Whang-Peng, J.3
Leventhal, B.G.4
-
31
-
-
0025893028
-
An estimate of the heritable fraction of childhood cancer
-
Narod SA, Stiller C, Lenoir GM (1991) An estimate of the heritable fraction of childhood cancer. Br J Cancer 63:993-999
-
(1991)
Br J Cancer
, vol.63
, pp. 993-999
-
-
Narod, S.A.1
Stiller, C.2
Lenoir, G.M.3
-
32
-
-
0026094584
-
Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome
-
Pelletier J, Bruening W, Kashtan CE, Mauer SM, Manivel JC, Striegel JZE, Houghton DC, et al (1991) Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome. Cell 87:437-447
-
(1991)
Cell
, vol.87
, pp. 437-447
-
-
Pelletier, J.1
Bruening, W.2
Kashtan, C.E.3
Mauer, S.M.4
Manivel, J.C.5
Striegel, J.Z.E.6
Houghton, D.C.7
-
33
-
-
0029022770
-
Rubinstein-Taybi syndrome caused by mutations in the transcriptional coactivator CBP
-
Petrij F, Giles R, Dauwerese HG, Saris JJ, Hennekam RCM, Masuno M, Tommerup N, et al (1995) Rubinstein-Taybi syndrome caused by mutations in the transcriptional coactivator CBP. Nature 376:348-351
-
(1995)
Nature
, vol.376
, pp. 348-351
-
-
Petrij, F.1
Giles, R.2
Dauwerese, H.G.3
Saris, J.J.4
Hennekam, R.C.M.5
Masuno, M.6
Tommerup, N.7
-
34
-
-
0017883401
-
Chromosomal imbalance in the aniridia-Wilms' tumour association: 11p interstitial deletion
-
Riccardi VM, Sujansky E, Smith AC, Francke U (1978) Chromosomal imbalance in the aniridia-Wilms' tumour association: 11p interstitial deletion. Pediatrics 61:604-610
-
(1978)
Pediatrics
, vol.61
, pp. 604-610
-
-
Riccardi, V.M.1
Sujansky, E.2
Smith, A.C.3
Francke, U.4
-
35
-
-
0020488518
-
Renal anomalies in childhood acute lymphoblastic leukemia
-
Robison LL, Swanson T, Day D, Ramsay NKC, L'Heureux P, Nesbit ME (1982) Renal anomalies in childhood acute lymphoblastic leukemia. N Engl J Med 307:1086-1087
-
(1982)
N Engl J Med
, vol.307
, pp. 1086-1087
-
-
Robison, L.L.1
Swanson, T.2
Day, D.3
Ramsay, N.K.C.4
L'Heureux, P.5
Nesbit, M.E.6
-
36
-
-
0023832163
-
Congenital anomalies associated with rhabdomyosarcoma: An autopsy study of 115 cases: A report from the International Rhabdomyosarcoma Study Committee
-
Ruymann FB, Maddux HR, Ragab A, Soule EH, Palmer N, Beltangady M, Gehan EA, et al (1988) Congenital anomalies associated with rhabdomyosarcoma: an autopsy study of 115 cases: a report from the International Rhabdomyosarcoma Study Committee. Med Pediatr Oncol 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
Gehan, E.A.7
-
37
-
-
0026552719
-
Association of rib anomalies and malignancy in childhood
-
Schumacher R, Mai A, Gutjahr P (1992) Association of rib anomalies and malignancy in childhood. Eur J Pediatr 151: 432-434
-
(1992)
Eur J Pediatr
, vol.151
, pp. 432-434
-
-
Schumacher, R.1
Mai, A.2
Gutjahr, P.3
-
38
-
-
0029586973
-
Childhood cancer in Britain: The National Registry of Childhood Tumour and incidence rates, 1978-87
-
Stiller CA, Allen MB, Eatock EM (1995) Childhood cancer in Britain: the National Registry of Childhood Tumour and incidence rates, 1978-87. Eur J Cancer Suppl 31A:2028-2034
-
(1995)
Eur J Cancer Suppl
, vol.31 A
, pp. 2028-2034
-
-
Stiller, C.A.1
Allen, M.B.2
Eatock, E.M.3
-
39
-
-
0023188919
-
Incidence of cardiac septal defects in children with Wilms' tumour and other malignant disease
-
Stiller CA, Lennox EL, Kinnier-Wilson LM (1987) Incidence of cardiac septal defects in children with Wilms' tumour and other malignant disease. Carcinogenesis 8:129-132
-
(1987)
Carcinogenesis
, vol.8
, pp. 129-132
-
-
Stiller, C.A.1
Lennox, E.L.2
Kinnier-Wilson, L.M.3
-
40
-
-
0014314248
-
The developmental defects associated with neuroblastoma-etiologic implications
-
Sy WM, Edmonsdon JH (1968) The developmental defects associated with neuroblastoma-etiologic implications. Cancer 22:234-238
-
(1968)
Cancer
, vol.22
, pp. 234-238
-
-
Sy, W.M.1
Edmonsdon, J.H.2
-
41
-
-
0026602124
-
Waardenburg syndrome (WS) patients have mutations in the human homologue of the Pax-3 paired box gene
-
Tassabehji M, Read AP, Newton VE, Harris R, Balling R, Gruss P, Strachan T (1992) Waardenburg syndrome (WS) patients have mutations in the human homologue of the Pax-3 paired box gene. Nature 355:635-636
-
(1992)
Nature
, vol.355
, pp. 635-636
-
-
Tassabehji, M.1
Read, A.P.2
Newton, V.E.3
Harris, R.4
Balling, R.5
Gruss, P.6
Strachan, T.7
-
43
-
-
0023341219
-
Familial glioma: Occurrence within the familial cancer syndrome and systemic malformations
-
Vieregge P, Gerhard L, Nahser HC (1987) Familial glioma: occurrence within the familial cancer syndrome and systemic malformations. J Neurol 234:220-232
-
(1987)
J Neurol
, vol.234
, pp. 220-232
-
-
Vieregge, P.1
Gerhard, L.2
Nahser, H.C.3
-
44
-
-
0027289089
-
Molecular characterization of cytogenetic alterations associated with Beckwith-Wiedemann syndrome (BWS) pheontype refines the localisation and suggests the gene for BWS is imprinted
-
Weksberg R, Teshima I, Williams B, Greenberg C, Pueschel S, Chernos J, Fawlow SB, et al (1993) Molecular characterization of cytogenetic alterations associated with Beckwith-Wiedemann syndrome (BWS) pheontype refines the localisation and suggests the gene for BWS is imprinted. Hum Mol Genet 2:549-556
-
(1993)
Hum Mol Genet
, vol.2
, pp. 549-556
-
-
Weksberg, R.1
Teshima, I.2
Williams, B.3
Greenberg, C.4
Pueschel, S.5
Chernos, J.6
Fawlow, S.B.7
-
45
-
-
34250134720
-
Tumors and hemihypertrophy associated with Wiedemann-Beckwith syndrome
-
Wiedemann HR (1983) Tumors and hemihypertrophy associated with Wiedemann-Beckwith syndrome. Eur J Pediatr 141:129
-
(1983)
Eur J Pediatr
, vol.141
, pp. 129
-
-
Wiedemann, H.R.1
-
46
-
-
0021911187
-
A population-based study of cancer incidence in twins and in children with congenital malformations or low birth weight, Norway, 1967-1980
-
Windham GC, Bjerkedal T, Langmark F (1985) A population-based study of cancer incidence in twins and in children with congenital malformations or low birth weight, Norway, 1967-1980. Am J Epidemiol 121:49-56
-
(1985)
Am J Epidemiol
, vol.121
, pp. 49-56
-
-
Windham, G.C.1
Bjerkedal, T.2
Langmark, F.3
|