-
1
-
-
0014337521
-
Hypertelorism with Turner phenotype: A new syndrome with associated congenital heart disease
-
Noonan JA. Hypertelorism with Turner phenotype: a new syndrome with associated congenital heart disease. Am J Dis Child 1968;16:373-80.
-
(1968)
Am J Dis Child
, vol.16
, pp. 373-380
-
-
Noonan, J.A.1
-
2
-
-
0028077697
-
Mapping a gene for Noonan's syndrome to the long arm of chromosome 12
-
Jamieson CR, van der Burgt I, Brady AF, et al. Mapping a gene for Noonan's syndrome to the long arm of chromosome 12. Nature Genet 1994;8:357-60.
-
(1994)
Nature Genet
, vol.8
, pp. 357-360
-
-
Jamieson, C.R.1
Van der Burgt, I.2
Brady, A.F.3
-
3
-
-
0031937054
-
Fine mapping of Noonan's cardiofacio-cutaneus-syndrome in a large family
-
Legius E, Schollen E, Matthijis G, et al. Fine mapping of Noonan's cardiofacio-cutaneus-syndrome in a large family. Europ J Hum Genet 1998;6:32-7.
-
(1998)
Europ J Hum Genet
, vol.6
, pp. 32-37
-
-
Legius, E.1
Schollen, E.2
Matthijis, G.3
-
4
-
-
18344385476
-
Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome
-
Tartaglia M, Mehler EL, Goldberg R, et al. Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome. Nat Genet 2001;29:465-8.
-
(2001)
Nat Genet
, vol.29
, pp. 465-468
-
-
Tartaglia, M.1
Mehler, E.L.2
Goldberg, R.3
-
5
-
-
0028127042
-
Clinical and molecular studies in a large Dutch family with Noonan's syndrome
-
van der Burgt I, Berends E, Lommen E, et al. Clinical and molecular studies in a large Dutch family with Noonan's syndrome. Am J Med Genet 1994;53:187-91.
-
(1994)
Am J Med Genet
, vol.53
, pp. 187-191
-
-
Van der Burgt, I.1
Berends, E.2
Lommen, E.3
-
6
-
-
2642651900
-
Noonan's syndrome associated with central giant cell granuloma
-
Ucar B, Okten A, Mocan H, et al. Noonan's syndrome associated with central giant cell granuloma. Clin Genet 1998;53:411-4.
-
(1998)
Clin Genet
, vol.53
, pp. 411-414
-
-
Ucar, B.1
Okten, A.2
Mocan, H.3
-
7
-
-
0034605374
-
Genetic heterogeneity in Noonan's syndrome: Evidence for an autosomal recessive form
-
van der Burgt I, Brunner H. Genetic heterogeneity in Noonan's syndrome: evidence for an autosomal recessive form. Am J Med Genet 2000;94:46-51.
-
(2000)
Am J Med Genet
, vol.94
, pp. 46-51
-
-
Van der Burgt, I.1
Brunner, H.2
-
8
-
-
0029027050
-
Vaginal rhabdomyosarcoma in a patient with Noonan's syndrome
-
Khan S, McDowell H, Upadhyaya M, et al. Vaginal rhabdomyosarcoma in a patient with Noonan's syndrome. J Med Genet 1995;32:743-5.
-
(1995)
J Med Genet
, vol.32
, pp. 743-745
-
-
Khan, S.1
McDowell, H.2
Upadhyaya, M.3
-
9
-
-
0035154736
-
Treatment of orbital rhabdomyosarcoma: Survival and late effects of treatment-results of an international workshop
-
Oberlin O, Rey A, Anderson J, et al. Treatment of orbital rhabdomyosarcoma: survival and late effects of treatment-results of an international workshop. J Clin Oncol 2001;19:197-204.
-
(2001)
J Clin Oncol
, vol.19
, pp. 197-204
-
-
Oberlin, O.1
Rey, A.2
Anderson, J.3
-
11
-
-
0032527329
-
"Benign" monoclonal gammopathy and chronic lymphatic leukemia in a patient with Noonan's syndrome
-
Riederer J. "Benign" monoclonal gammopathy and chronic lymphatic leukemia in a patient with Noonan's syndrome. Med Klin 1998;93:433-7.
-
(1998)
Med Klin
, vol.93
, pp. 433-437
-
-
Riederer, J.1
-
12
-
-
0030712155
-
Occurrence of myeloproliferative disorder in patient with Noonan's syndrome
-
Bader-Meunier B, Tchernia G, Mielot F, et al. Occurrence of myeloproliferative disorder in patient with Noonan's syndrome. J Pediatr 1997;130:885-9.
-
(1997)
J Pediatr
, vol.130
, pp. 885-889
-
-
Bader-Meunier, B.1
Tchernia, G.2
Mielot, F.3
-
13
-
-
0030973928
-
Noonan's syndrome associated with neuroblastoma: A case report
-
Lopez-Miranda B, Westra SJ, Yazdani S, et al. Noonan's syndrome associated with neuroblastoma: a case report. Pediatr Radiol 1997;27:324-6.
-
(1997)
Pediatr Radiol
, vol.27
, pp. 324-326
-
-
Lopez-Miranda, B.1
Westra, S.J.2
Yazdani, S.3
-
14
-
-
0025821019
-
Noonan-like multiple giant cell lesion syndrome
-
Cohen MM Jr, Gorlin RJ. Noonan-like multiple giant cell lesion syndrome. Am J Med Genet 1991;40:159-66.
-
(1991)
Am J Med Genet
, vol.40
, pp. 159-166
-
-
Cohen M.M., Jr.1
Gorlin, R.J.2
-
15
-
-
0032559129
-
Neurofibromatosis-Noonan's syndrome
-
Carey JC. Neurofibromatosis-Noonan's syndrome. Am J Med Genet 1998;75:263-4.
-
(1998)
Am J Med Genet
, vol.75
, pp. 263-264
-
-
Carey, J.C.1
-
16
-
-
0023477995
-
Differential diagnosis of posterior cervical hygroma in previable fetuses
-
Kalousek DK, Sleer MJ. Differential diagnosis of posterior cervical hygroma in previable fetuses. Am J Med Genet 1987; Suppl 3:83-92.
-
(1987)
Am J Med Genet
, Issue.SUPPL. 3
, pp. 83-92
-
-
Kalousek, D.K.1
Sleer, M.J.2
-
17
-
-
0033503449
-
Rhabdomyosarcoma in a patient with cardio-facio-cutaneus syndrome
-
Bisogno G, Murgia A, Mammi I, et al. Rhabdomyosarcoma in a patient with cardio-facio-cutaneus syndrome. J Pediatr Hematol Oncol 1999;21:424-7.
-
(1999)
J Pediatr Hematol Oncol
, vol.21
, pp. 424-427
-
-
Bisogno, G.1
Murgia, A.2
Mammi, I.3
-
18
-
-
0031757257
-
Costello syndrome: Two cases with embryonal rhabdomyosarcoma
-
Kerr B, Eden OB, Dandamudi R, et al. Costello syndrome: two cases with embryonal rhabdomyosarcoma. J Med Genet 1998;35:1036-9.
-
(1998)
J Med Genet
, vol.35
, pp. 1036-1039
-
-
Kerr, B.1
Eden, O.B.2
Dandamudi, R.3
-
19
-
-
0032966589
-
Costello syndrome and rhabdomyosarcoma
-
Feingold M. Costello syndrome and rhabdomyosarcoma. J Med Genet 1999;36:582-3.
-
(1999)
J Med Genet
, vol.36
, pp. 582-583
-
-
Feingold, M.1
-
20
-
-
0035931430
-
Are Noonan syndrome and Noonan-like syndrome/multiple giant cell lesion syndrome distinct entities?
-
Bertola DR, Kim ChA, Pereira AC, et al. Are Noonan syndrome and Noonan-like syndrome/multiple giant cell lesion syndrome distinct entities? Am J Med Genet 2001;98:230-4.
-
(2001)
Am J Med Genet
, vol.98
, pp. 230-234
-
-
Bertola, D.R.1
Kim, Ch.A.2
Pereira, A.C.3
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