-
1
-
-
0035166566
-
Course and outcome of a pregnancy with a giant fetal cervical teratoma diagnosed prenatally
-
Axt-Fliedner R, Hendrik H-J, Ertan K, et al. 2001. Course and outcome of a pregnancy with a giant fetal cervical teratoma diagnosed prenatally. Ultrasound Obstet Gynecol 18:543-546.
-
(2001)
Ultrasound Obstet Gynecol
, vol.18
, pp. 543-546
-
-
Axt-Fliedner, R.1
Hendrik, H.-J.2
Ertan, K.3
-
2
-
-
0033229987
-
Nasopharyngeal teratoma and mosaic tetrasomy 1q detected at amniocentesis. A case report and review of the literature
-
Beverstock GC, Mollevanger P, Baaij M, et al. 1999. Nasopharyngeal teratoma and mosaic tetrasomy 1q detected at amniocentesis. A case report and review of the literature. Cancer Genet Cytogenet 115:11-18.
-
(1999)
Cancer Genet Cytogenet
, vol.115
, pp. 11-18
-
-
Beverstock, G.C.1
Mollevanger, P.2
Baaij, M.3
-
3
-
-
0346749431
-
High-resolution analysis of genetic events in cancer cells using bacterial artificial chromosome arrays and comparative genomic hybridisation
-
Cowell JK, Nowak NJ. 2003. High-resolution analysis of genetic events in cancer cells using bacterial artificial chromosome arrays and comparative genomic hybridisation. Adv Cancer Res 90:91-125.
-
(2003)
Adv Cancer Res
, vol.90
, pp. 91-125
-
-
Cowell, J.K.1
Nowak, N.J.2
-
4
-
-
0842266542
-
Characterization of the 1p/19q chromosomal loss in oligodendrogliomas using comparative genomic hybridization arrays (CGHa)
-
Cowell JK, Barnett GH, Nowak NJ. 2004a. Characterization of the 1p/19q chromosomal loss in oligodendrogliomas using comparative genomic hybridization arrays (CGHa). J Neuropathol Exp Neurol 63:151-158.
-
(2004)
J Neuropathol Exp Neurol
, vol.63
, pp. 151-158
-
-
Cowell, J.K.1
Barnett, G.H.2
Nowak, N.J.3
-
5
-
-
2342468007
-
Application of bacterial artificial chromosome array-based comparative genomic hybridization and spectral karyotyping to the analysis of glioblastoma multiforme
-
Cowell JK, Matsui S, Wang YD, et al. 2004b. Application of bacterial artificial chromosome array-based comparative genomic hybridization and spectral karyotyping to the analysis of glioblastoma multiforme. Cancer Genet Cytogenet 151:36-51.
-
(2004)
Cancer Genet Cytogenet
, vol.151
, pp. 36-51
-
-
Cowell, J.K.1
Matsui, S.2
Wang, Y.D.3
-
6
-
-
1642267572
-
Identification and characterisation of constitutional chromosome abnormalities using arrays of bacterial artificial chromosomes
-
Cowell JK, Wang YD, Head K, et al. 2004c. Identification and characterisation of constitutional chromosome abnormalities using arrays of bacterial artificial chromosomes. Br J Cancer 90:860-865.
-
(2004)
Br J Cancer
, vol.90
, pp. 860-865
-
-
Cowell, J.K.1
Wang, Y.D.2
Head, K.3
-
7
-
-
0036079961
-
The leukemia-associated gene Mllt1/ENL: Characterization of a murine homolog and demonstration of an essential role in embryonic development
-
Doty RT, Vanasse GJ, Disteche CM, Willerford DM. 2002. The leukemia-associated gene Mllt1/ENL: characterization of a murine homolog and demonstration of an essential role in embryonic development. Blood Cells Mol Dis 28:407-417.
-
(2002)
Blood Cells Mol Dis
, vol.28
, pp. 407-417
-
-
Doty, R.T.1
Vanasse, G.J.2
Disteche, C.M.3
Willerford, D.M.4
-
8
-
-
0017178250
-
Benign and malignant teratomas in children: Analysis of 85 patients
-
Grosfeld JL, Ballantine TVN, Lowe D, Baehner RL. 1976. Benign and malignant teratomas in children: analysis of 85 patients. Surgery 80:297-305.
-
(1976)
Surgery
, vol.80
, pp. 297-305
-
-
Grosfeld, J.L.1
Ballantine, T.V.N.2
Lowe, D.3
Baehner, R.L.4
-
9
-
-
0029087037
-
Down's syndrome associated with intracranial germinoma and testicular embryonal carcinoma
-
Hashimoto T, Sasagawa I, Ishigooka M, et al. 1995. Down's syndrome associated with intracranial germinoma and testicular embryonal carcinoma. Urol Int 55:120-122.
-
(1995)
Urol Int
, vol.55
, pp. 120-122
-
-
Hashimoto, T.1
Sasagawa, I.2
Ishigooka, M.3
-
10
-
-
0021328067
-
Direct prenatal chromosome diagnosis of a malignancy
-
Hecht F, Grix A, Hecht BK, et al. 1984. Direct prenatal chromosome diagnosis of a malignancy. Cancer Genet Cytogenet 11:107-111.
-
(1984)
Cancer Genet Cytogenet
, vol.11
, pp. 107-111
-
-
Hecht, F.1
Grix, A.2
Hecht, B.K.3
-
11
-
-
0034094639
-
Congenital sacrococcygeal teratomas: Effect of gestational age on size, morphologic pattern, ploidy, p53, and ret expression
-
Hermann ME, Thomson K, Wojcik EM, et al. 2000. Congenital sacrococcygeal teratomas: effect of gestational age on size, morphologic pattern, ploidy, p53, and ret expression. Pediatr Dev Pathol 3:240-248.
-
(2000)
Pediatr Dev Pathol
, vol.3
, pp. 240-248
-
-
Hermann, M.E.1
Thomson, K.2
Wojcik, E.M.3
-
12
-
-
0009502086
-
Trisomy 1q associated with fetal cervical teratoma
-
Abstract
-
Hirata GI, Millar LK, Donlon SS, et al. 1994. Trisomy 1q associated with fetal cervical teratoma. [Abstract] Am J Med Genet 52:373-374.
-
(1994)
Am J Med Genet
, vol.52
, pp. 373-374
-
-
Hirata, G.I.1
Millar, L.K.2
Donlon, S.S.3
-
13
-
-
4444291843
-
Detection of large-scale variation in the human genome
-
Iafrate AJ, Feuk L, Rivera MN, et al. 2004. Detection of large-scale variation in the human genome. Nat Genet 36:949-951.
-
(2004)
Nat Genet
, vol.36
, pp. 949-951
-
-
Iafrate, A.J.1
Feuk, L.2
Rivera, M.N.3
-
14
-
-
0031973233
-
Cervical teratoma: Prenatal diagnosis and long-term follow-up
-
Kerner B, Flaum E, Mathews H, et al. 1998. Cervical teratoma: prenatal diagnosis and long-term follow-up. Prenat Diagn 18:51-59.
-
(1998)
Prenat Diagn
, vol.18
, pp. 51-59
-
-
Kerner, B.1
Flaum, E.2
Mathews, H.3
-
16
-
-
0034889575
-
The mechanism of palatal clefting in the Col11a1 mutant mouse
-
Lavrin IO, McLean W, Seegmiller RE, et al. 2001. The mechanism of palatal clefting in the Col11a1 mutant mouse. Arch Oral Biol 46:865-869.
-
(2001)
Arch Oral Biol
, vol.46
, pp. 865-869
-
-
Lavrin, I.O.1
McLean, W.2
Seegmiller, R.E.3
-
17
-
-
0348108093
-
Prenatal diagnosis of sacrococcygeal teratoma with constitutional partial monosomy 7q/trisomy 2p
-
Le Caignec C, Winer N, Boceno M, et al. 2003. Prenatal diagnosis of sacrococcygeal teratoma with constitutional partial monosomy 7q/trisomy 2p. Prenat Diagn 23:981-984.
-
(2003)
Prenat Diagn
, vol.23
, pp. 981-984
-
-
Le Caignec, C.1
Winer, N.2
Boceno, M.3
-
18
-
-
0016795110
-
Origin of extragonadal teratomas and endodermal sinus tumors
-
Linder D, Hecht F, McCaw BK, Campbell JR. 1975. Origin of extragonadal teratomas and endodermal sinus tumors. Nature 254:597-598.
-
(1975)
Nature
, vol.254
, pp. 597-598
-
-
Linder, D.1
Hecht, F.2
McCaw, B.K.3
Campbell, J.R.4
-
19
-
-
0032989692
-
Pathogenesis of testicular germ cell tumours
-
Looijenga LHJ, Oosterhuis JW. 1999. Pathogenesis of testicular germ cell tumours. Rev Reprod 4:90-100
-
(1999)
Rev Reprod
, vol.4
, pp. 90-100
-
-
Looijenga, L.H.J.1
Oosterhuis, J.W.2
-
20
-
-
0242417624
-
Collagen XI sequence variations in nonsyndromic cleft palate, Robin sequence and micrognathia
-
Melkoniemi M, Koillinen H, Mannikko M, et al. 2003. Collagen XI sequence variations in nonsyndromic cleft palate, Robin sequence and micrognathia. Eur J Hum Genet 11:265-270.
-
(2003)
Eur J Hum Genet
, vol.11
, pp. 265-270
-
-
Melkoniemi, M.1
Koillinen, H.2
Mannikko, M.3
-
22
-
-
0345059312
-
Sequence variations in the collagen IX and XI genes are associated with degenerative lumbar spinal stenosis
-
Noponen-Hietala N, Kyllonen E, Mannikko M, et al. 2003. Sequence variations in the collagen IX and XI genes are associated with degenerative lumbar spinal stenosis. Ann Rheum Dis 62:1208-1214.
-
(2003)
Ann Rheum Dis
, vol.62
, pp. 1208-1214
-
-
Noponen-Hietala, N.1
Kyllonen, E.2
Mannikko, M.3
-
23
-
-
0034981607
-
Stickler syndrome and vitreoretinal degeneration: Correlation between locus mutation and vitreous phenotype. Apropos of a case
-
Parentin F, Sangalli A, Mottes M, Perissutti P. 2001. Stickler syndrome and vitreoretinal degeneration: correlation between locus mutation and vitreous phenotype. Apropos of a case. Graefes Arch Clin Exp Ophthalmol 239:316-319.
-
(2001)
Graefes Arch Clin Exp Ophthalmol
, vol.239
, pp. 316-319
-
-
Parentin, F.1
Sangalli, A.2
Mottes, M.3
Perissutti, P.4
-
24
-
-
0036863497
-
No chromosomal imbalances detected by comparative genomic hybridization in a case of fetal immature teratoma
-
Rickert CH, Paulus W. 2002. No chromosomal imbalances detected by comparative genomic hybridization in a case of fetal immature teratoma. Childs Nerv Syst 18:639-643.
-
(2002)
Childs Nerv Syst
, vol.18
, pp. 639-643
-
-
Rickert, C.H.1
Paulus, W.2
-
25
-
-
0030794910
-
Radiologic-pathologic conference of Children's Hospital Boston: Pineal region mass in a neonate
-
Robson CD, Price DL, Barnes PD, Taylor GA. 1997. Radiologic-pathologic conference of Children's Hospital Boston: pineal region mass in a neonate. Pediatr Radiol 27:829-831.
-
(1997)
Pediatr Radiol
, vol.27
, pp. 829-831
-
-
Robson, C.D.1
Price, D.L.2
Barnes, P.D.3
Taylor, G.A.4
-
26
-
-
0033230453
-
Isochromosome 1q as the sole chromosomal abnormality in two fetal teratomas: Possible trisomic or tetrasomic zygote rescue in fetal teratoma with an additional isochromosome 1q
-
Scheres JMJC, de Pater JM, Stoutenbeek P, et al. 1999. Isochromosome 1q as the sole chromosomal abnormality in two fetal teratomas: possible trisomic or tetrasomic zygote rescue in fetal teratoma with an additional isochromosome 1q. Cancer Genet Cytogenet 115:1-10.
-
(1999)
Cancer Genet Cytogenet
, vol.115
, pp. 1-10
-
-
Scheres, J.M.J.C.1
De Pater, J.M.2
Stoutenbeek, P.3
-
27
-
-
0026731146
-
An unusual mosaic karyotype detected through prenatal diagnosis with duplication of 1q and 19p and associated teratoma development
-
Schwartz S, Raffel LJ, Sun C-CJ, Waters E. 1992. An unusual mosaic karyotype detected through prenatal diagnosis with duplication of 1q and 19p and associated teratoma development. Teratology 46:399-404.
-
(1992)
Teratology
, vol.46
, pp. 399-404
-
-
Schwartz, S.1
Raffel, L.J.2
Sun, C.-C.J.3
Waters, E.4
-
28
-
-
0035179871
-
Assembly of microarrays for genome-wide measurement of DNA copy number by CGH
-
Snidjers A, Nowak N, Seagraves R, et al. 2001. Assembly of microarrays for genome-wide measurement of DNA copy number by CGH. Nat Genet 29:263-264.
-
(2001)
Nat Genet
, vol.29
, pp. 263-264
-
-
Snidjers, A.1
Nowak, N.2
Seagraves, R.3
-
29
-
-
0020573632
-
Teratomas in infancy and childhood. A 54-year experience at the Children's Hospital Medical Center
-
Tapper D, Lack EE. 1983. Teratomas in infancy and childhood. A 54-year experience at the Children's Hospital Medical Center. Ann Surg 198:398-409.
-
(1983)
Ann Surg
, vol.198
, pp. 398-409
-
-
Tapper, D.1
Lack, E.E.2
-
31
-
-
0021637239
-
Prenatal ultrasound diagnosis of fetal teratomas of the neck
-
Trecet JC, Claramunt V, Larraz J, et al. 1984. Prenatal ultrasound diagnosis of fetal teratomas of the neck. J Clin Ultrasound 12:509-511.
-
(1984)
J Clin Ultrasound
, vol.12
, pp. 509-511
-
-
Trecet, J.C.1
Claramunt, V.2
Larraz, J.3
-
32
-
-
0037242383
-
The MYST family of histone acetyltransferases
-
Utley RT, Cote J. 2003. The MYST family of histone acetyltransferases. Curr Top Microbiol Immunol 274:203-236.
-
(2003)
Curr Top Microbiol Immunol
, vol.274
, pp. 203-236
-
-
Utley, R.T.1
Cote, J.2
-
33
-
-
0038222520
-
Germ cell tumours in neonates and infants: A distinct subgroup?
-
Veltman IM, Schepens MT, Looijenga LHJ, et al. 2003. Germ cell tumours in neonates and infants: a distinct subgroup? APMIS 111:152-60.
-
(2003)
APMIS
, vol.111
, pp. 152-160
-
-
Veltman, I.M.1
Schepens, M.T.2
Looijenga, L.H.J.3
-
34
-
-
0028201808
-
The MLLT3 gene maps between D9S156 and D9S171 and contains an unstable polymorphic trinucleotide repeat
-
Walker GJ, Walters MK, Plamer JM, Hayward NK. 1994. The MLLT3 gene maps between D9S156 and D9S171 and contains an unstable polymorphic trinucleotide repeat. Genomics 20:490-491.
-
(1994)
Genomics
, vol.20
, pp. 490-491
-
-
Walker, G.J.1
Walters, M.K.2
Plamer, J.M.3
Hayward, N.K.4
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