-
1
-
-
0026799274
-
Anticipation in myotonic dystrophy
-
Ashizawa T, Dunne CJ, Dubel JR, Perryman MB, Epstein HF, Boerwinkle E, Hejtmancik JF (1992) Anticipation in myotonic dystrophy. Neurology 42:1871-1877
-
(1992)
Neurology
, vol.42
, pp. 1871-1877
-
-
Ashizawa, T.1
Dunne, C.J.2
Dubel, J.R.3
Perryman, M.B.4
Epstein, H.F.5
Boerwinkle, E.6
Hejtmancik, J.F.7
-
2
-
-
0029587022
-
Gametic imprinting in mammals
-
Barlow D (1995) Gametic imprinting in mammals. Science 270: 1610-1613
-
(1995)
Science
, vol.270
, pp. 1610-1613
-
-
Barlow, D.1
-
4
-
-
0025863603
-
Parental-specific methylation of an imprinted transgene is established during gametogenesis and progressively changes during embryogenesis
-
Chaillet JR, Vogt TF, Beier DR, Leder P (1991) Parental-specific methylation of an imprinted transgene is established during gametogenesis and progressively changes during embryogenesis. Cell 66:77-83
-
(1991)
Cell
, vol.66
, pp. 77-83
-
-
Chaillet, J.R.1
Vogt, T.F.2
Beier, D.R.3
Leder, P.4
-
5
-
-
0028917187
-
Parents do matter: Genomic imprinting and parental sex effects in neurological disorders
-
Chatkupt S, Antonowicz M, Johnson WG (1995) Parents do matter: genomic imprinting and parental sex effects in neurological disorders. J Neurol Sci 130:1-10
-
(1995)
J Neurol Sci
, vol.130
, pp. 1-10
-
-
Chatkupt, S.1
Antonowicz, M.2
Johnson, W.G.3
-
8
-
-
0027937412
-
Allelotype of head and neck paragangliomas: Allelic imbalance is confined to the long arm of chromosome 11, the site of the predisposing locus PGL
-
Devilee P, van Schothorst EM, Bardoel AF, Bonsing B, Kuipers-Dijkshoorn N, James MR, Fleuren G, et al (1994) Allelotype of head and neck paragangliomas: allelic imbalance is confined to the long arm of chromosome 11, the site of the predisposing locus PGL. Genes Chromosom Cancer 11:71-78
-
(1994)
Genes Chromosom Cancer
, vol.11
, pp. 71-78
-
-
Devilee, P.1
Van Schothorst, E.M.2
Bardoel, A.F.3
Bonsing, B.4
Kuipers-Dijkshoorn, N.5
James, M.R.6
Fleuren, G.7
-
9
-
-
13344259999
-
A comprehensive genetic map of the human genome based on 5,264 microsatellites
-
Dib C, Faure S, Fizames C, Samson D, Drouot N, Vignal A, Millasseau P, et al (1996) A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 380:152-154
-
(1996)
Nature
, vol.380
, pp. 152-154
-
-
Dib, C.1
Faure, S.2
Fizames, C.3
Samson, D.4
Drouot, N.5
Vignal, A.6
Millasseau, P.7
-
10
-
-
0027981726
-
Is there evidence for anticipation in autosomal dominant polycystic kidney disease?
-
Fick GM, Johnson AM, Gabow P (1994) Is there evidence for anticipation in autosomal dominant polycystic kidney disease? Kidney Int 45:1153-1162
-
(1994)
Kidney Int
, vol.45
, pp. 1153-1162
-
-
Fick, G.M.1
Johnson, A.M.2
Gabow, P.3
-
11
-
-
0027477595
-
Loss of heterozygosity and amplification of chromosome 11q in human ovarian cancer
-
Foulkes WD, Campbell IG, Stamp GWH, Trowsdale J (1993) Loss of heterozygosity and amplification of chromosome 11q in human ovarian cancer. Br J Cancer 67:268-273
-
(1993)
Br J Cancer
, vol.67
, pp. 268-273
-
-
Foulkes, W.D.1
Campbell, I.G.2
Stamp, G.W.H.3
Trowsdale, J.4
-
12
-
-
0018976591
-
Familial carotid body tumors: Case report and epidemiological review
-
Grufferman S, Gillman MW, Pasternak LR, Peterson CL, Young WG (1980) Familial carotid body tumors: case report and epidemiological review. Cancer 46:2116-2122
-
(1980)
Cancer
, vol.46
, pp. 2116-2122
-
-
Grufferman, S.1
Gillman, M.W.2
Pasternak, L.R.3
Peterson, C.L.4
Young, W.G.5
-
13
-
-
0001076782
-
Parent-specific gene expression and the triploid endosperm
-
Haig D, Westoby M (1989) Parent-specific gene expression and the triploid endosperm. Am Nat 134:147-155
-
(1989)
Am Nat
, vol.134
, pp. 147-155
-
-
Haig, D.1
Westoby, M.2
-
14
-
-
0028123002
-
Loss of heterozygosity in sporadic human breast carcinoma: A common region between 11q22 and 11q23.3
-
Hampton GM, Mannermaa A, Winquist R, Alavaikko M, Blanco G, Taskinen PJ, Kiviniemi H, et al (1994a) Loss of heterozygosity in sporadic human breast carcinoma: a common region between 11q22 and 11q23.3. Cancer Res 54:4586-4589
-
(1994)
Cancer Res
, vol.54
, pp. 4586-4589
-
-
Hampton, G.M.1
Mannermaa, A.2
Winquist, R.3
Alavaikko, M.4
Blanco, G.5
Taskinen, P.J.6
Kiviniemi, H.7
-
15
-
-
0028365264
-
Loss of heterozygosity in cervical carcinoma: Subchromosomal localization of a putative tumor-suppressor gene to chromosome 11q22-q24
-
Hampton GM, Penny LA, Baergen RN, Larson A, Brewer C, Liao S, Busby-Earle RM, et al (1994b) Loss of heterozygosity in cervical carcinoma: subchromosomal localization of a putative tumor-suppressor gene to chromosome 11q22-q24. Proc Natl Acad Sci USA 91:6953-6957
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 6953-6957
-
-
Hampton, G.M.1
Penny, L.A.2
Baergen, R.N.3
Larson, A.4
Brewer, C.5
Liao, S.6
Busby-Earle, R.M.7
-
16
-
-
0029002574
-
A defined region of loss of heterozygosity at 11q23 in cutaneous malignant melanoma
-
Herbst RA, Larson A, Weiss J, Cavenee WK, Hampton GM, Arden KC (1995) A defined region of loss of heterozygosity at 11q23 in cutaneous malignant melanoma. Cancer Res 55:2494-2496
-
(1995)
Cancer Res
, vol.55
, pp. 2494-2496
-
-
Herbst, R.A.1
Larson, A.2
Weiss, J.3
Cavenee, W.K.4
Hampton, G.M.5
Arden, K.C.6
-
17
-
-
0026849378
-
A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter
-
Heutink P, van der Mey AG, Sandkuijl LA, van Gils AP, Bardoel A, Breedveld GJ, van Vliet M, et al (1992) A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter. Hum Mol Genet 1:7-10
-
(1992)
Hum Mol Genet
, vol.1
, pp. 7-10
-
-
Heutink, P.1
Van Der Mey, A.G.2
Sandkuijl, L.A.3
Van Gils, A.P.4
Bardoel, A.5
Breedveld, G.J.6
Van Vliet, M.7
-
18
-
-
0028142934
-
Further localization of the gene for hereditary paragangliomas and evidence for linkage in unrelated families
-
Heutink P, van Schothorst EM, van der Mey AG, Bardoel A, Breedveld G, Pertijs J, Sandkuijl LA, et al (1994) Further localization of the gene for hereditary paragangliomas and evidence for linkage in unrelated families. Eur J Hum Genet 2:148-158
-
(1994)
Eur J Hum Genet
, vol.2
, pp. 148-158
-
-
Heutink, P.1
Van Schothorst, E.M.2
Van Der Mey, A.G.3
Bardoel, A.4
Breedveld, G.5
Pertijs, J.6
Sandkuijl, L.A.7
-
19
-
-
0029103432
-
Statistical pitfalls in detecting age-of-onset anticipation: The role of correlation in studying anticipation and detecting ascertainment bias
-
Hodge SE, Wickramaratne P (1995) Statistical pitfalls in detecting age-of-onset anticipation: the role of correlation in studying anticipation and detecting ascertainment bias. Psychiatr Genet 5:43-47
-
(1995)
Psychiatr Genet
, vol.5
, pp. 43-47
-
-
Hodge, S.E.1
Wickramaratne, P.2
-
20
-
-
13344278697
-
Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments
-
Hoovers JMN, Kalikin LM, Johnson LA, Alders M, Redeker B, Law DJ, Bliek J, et al (1995) Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments. Proc Natl Acad Sci USA 92: 12456-12460
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 12456-12460
-
-
Hoovers, J.M.N.1
Kalikin, L.M.2
Johnson, L.A.3
Alders, M.4
Redeker, B.5
Law, D.J.6
Bliek, J.7
-
21
-
-
0024390849
-
Anticipation in myotonic dystrophy: Fact or fiction?
-
Howeler CJ, Busch HFM, Geraedts JPM, Niermeijer MF, Staal A (1989) Anticipation in myotonic dystrophy: fact or fiction? Brain 112:779-797
-
(1989)
Brain
, vol.112
, pp. 779-797
-
-
Howeler, C.J.1
Busch, H.F.M.2
Geraedts, J.P.M.3
Niermeijer, M.F.4
Staal, A.5
-
23
-
-
0029010787
-
Allelic losses in human chromosome 11 in lung cancers
-
Iizuka M, Sugiyama Y, Shiraishi M, Jones C, Sekiya T (1995) Allelic losses in human chromosome 11 in lung cancers. Genes Chromosom Cancer 13:40-46
-
(1995)
Genes Chromosom Cancer
, vol.13
, pp. 40-46
-
-
Iizuka, M.1
Sugiyama, Y.2
Shiraishi, M.3
Jones, C.4
Sekiya, T.5
-
24
-
-
20244377832
-
A radiation hybrid map of 506 STS markers spanning human chromosome 11
-
James MR, Richard CW III, Schott J-J, Yousry C, Clark K, Bell J, Terwilliger JD, et al (1994) A radiation hybrid map of 506 STS markers spanning human chromosome 11. Nat Genet 7:70-76
-
(1994)
Nat Genet
, vol.7
, pp. 70-76
-
-
James, M.R.1
Richard III, C.W.2
Schott, J.-J.3
Yousry, C.4
Clark, K.5
Bell, J.6
Terwilliger, J.D.7
-
25
-
-
0027515936
-
11q deletions in human colorectal carcinomas: Cytogenetics and restriction fragment length polymorphism analysis
-
Keldysh PL, Dragani TA, Fleischman EW, Konstantinova LN, Perevoschikov AG, Pierotti MA, Della Porta G, et al (1993) 11q deletions in human colorectal carcinomas: cytogenetics and restriction fragment length polymorphism analysis. Genes Chromosom Cancer. 6:45-50
-
(1993)
Genes Chromosom Cancer
, vol.6
, pp. 45-50
-
-
Keldysh, P.L.1
Dragani, T.A.2
Fleischman, E.W.3
Konstantinova, L.N.4
Perevoschikov, A.G.5
Pierotti, M.A.6
Della Porta, G.7
-
26
-
-
0023024017
-
Genetics of human cancer
-
Knudson AG (1986) Genetics of human cancer. Annu Rev Genet 20:231-251
-
(1986)
Annu Rev Genet
, vol.20
, pp. 231-251
-
-
Knudson, A.G.1
-
27
-
-
0027231784
-
Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from chromosome 11
-
Koi M, Johnson LA, Kalikin LM, Little PFR, Nakamura Y, Feinberg AP (1993) Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from chromosome 11. Science 260:361-364
-
(1993)
Science
, vol.260
, pp. 361-364
-
-
Koi, M.1
Johnson, L.A.2
Kalikin, L.M.3
Little, P.F.R.4
Nakamura, Y.5
Feinberg, A.P.6
-
28
-
-
0002921028
-
Hereditary deficiencies of clotting factors VII and X associated with carotid body tumors
-
Kroll AJ, Alexander B, Cochios F, Pechet L (1964) Hereditary deficiencies of clotting factors VII and X associated with carotid body tumors. N Engl J Med 270:6-13
-
(1964)
N Engl J Med
, vol.270
, pp. 6-13
-
-
Kroll, A.J.1
Alexander, B.2
Cochios, F.3
Pechet, L.4
-
29
-
-
0028809123
-
Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1: Evidence for genetic heterogeneity
-
Mariman EC, van Beersum SE, Cremers CW, Struycken PM, Ropers HH (1995) Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1: evidence for genetic heterogeneity. Hum Genet 95:56-62
-
(1995)
Hum Genet
, vol.95
, pp. 56-62
-
-
Mariman, E.C.1
Van Beersum, S.E.2
Cremers, C.W.3
Struycken, P.M.4
Ropers, H.H.5
-
30
-
-
0027190801
-
Analysis of a second family with hereditary non-chromaffin paragangliomas locates the underlying gene at the proximal region of chromosome 11q
-
Mariman EC, van Beersum SE, Cremers CW, van Baars FM, Ropers HH (1993) Analysis of a second family with hereditary non-chromaffin paragangliomas locates the underlying gene at the proximal region of chromosome 11q. Hum Genet 91:357-361
-
(1993)
Hum Genet
, vol.91
, pp. 357-361
-
-
Mariman, E.C.1
Van Beersum, S.E.2
Cremers, C.W.3
Van Baars, F.M.4
Ropers, H.H.5
-
31
-
-
0028032392
-
Familial paragangliomas of the head and neck
-
McCaffrey TV, Meyer FB, Michels W, Piepgras DG, Marion MS (1994) Familial paragangliomas of the head and neck. Arch Otolaryngol Head Neck Surg 120:1211-1216
-
(1994)
Arch Otolaryngol Head Neck Surg
, vol.120
, pp. 1211-1216
-
-
McCaffrey, T.V.1
Meyer, F.B.2
Michels, W.3
Piepgras, D.G.4
Marion, M.S.5
-
32
-
-
0028227938
-
Epigenetic lesions at the H19 locus in Wilms tumor patients
-
Moulton T, Crenshaw T, Hao Y, Moosikasuwan J, Lin N, Dembitzer F, Hensle T, et al (1994) Epigenetic lesions at the H19 locus in Wilms tumor patients. Nat Genet 7:440-447
-
(1994)
Nat Genet
, vol.7
, pp. 440-447
-
-
Moulton, T.1
Crenshaw, T.2
Hao, Y.3
Moosikasuwan, J.4
Lin, N.5
Dembitzer, F.6
Hensle, T.7
-
33
-
-
0029012254
-
Definition and refinement of chromosome 11 regions of loss of heterozygosity in breast cancer: Identification of a new region at 11q23.3
-
Negrini M, Rasio D, Hampton GM, Sabbioni S, Rattan S, Carter SL, Rosenberg AL, et al (1995) Definition and refinement of chromosome 11 regions of loss of heterozygosity in breast cancer: identification of a new region at 11q23.3. Cancer Res 55:3003-3007
-
(1995)
Cancer Res
, vol.55
, pp. 3003-3007
-
-
Negrini, M.1
Rasio, D.2
Hampton, G.M.3
Sabbioni, S.4
Rattan, S.5
Carter, S.L.6
Rosenberg, A.L.7
-
34
-
-
0028790963
-
The VITESSE algorithm for rapid multilocus linkage analysis via genotype set-recoding and fuzzy inheritance
-
O'Connell JR, Weeks DE (1995) The VITESSE algorithm for rapid multilocus linkage analysis via genotype set-recoding and fuzzy inheritance. Nat Genet 11:402-408
-
(1995)
Nat Genet
, vol.11
, pp. 402-408
-
-
O'Connell, J.R.1
Weeks, D.E.2
-
35
-
-
0019968970
-
Carotid body tumors in humans: Genetics and epidemiology
-
Parry DM, Li FP, Strong LC, Carney JA, Schottenfeld D, Reimer RR, Grufferman S (1982) Carotid body tumors in humans: genetics and epidemiology. J Natl Cancer Inst 68: 573-578
-
(1982)
J Natl Cancer Inst
, vol.68
, pp. 573-578
-
-
Parry, D.M.1
Li, F.P.2
Strong, L.C.3
Carney, J.A.4
Schottenfeld, D.5
Reimer, R.R.6
Grufferman, S.7
-
36
-
-
9044227621
-
Localization of a tumor suppressor gene in 11p15.5 using the G401 Wilms tumor assay
-
Reid LH, West A, Gioeli DG, Phillips KK, Kelleher KF, Araujo D, Stanbridge EJ, et al (1996) Localization of a tumor suppressor gene in 11p15.5 using the G401 Wilms tumor assay. Hum Mol Genet 5:239-248
-
(1996)
Hum Mol Genet
, vol.5
, pp. 239-248
-
-
Reid, L.H.1
West, A.2
Gioeli, D.G.3
Phillips, K.K.4
Kelleher, K.F.5
Araujo, D.6
Stanbridge, E.J.7
-
37
-
-
0028139060
-
Parental origin effects, genome imprinting, and sex-ratio distortion: Double or nothing?
-
Sapienza C (1994) Parental origin effects, genome imprinting, and sex-ratio distortion: double or nothing? Am J Hum Genet 55:1073-1075
-
(1994)
Am J Hum Genet
, vol.55
, pp. 1073-1075
-
-
Sapienza, C.1
-
38
-
-
0001772537
-
Genome imprinting in human disease
-
Scriver CR, Beaudet AL, Sly WS, Valle D (eds) McGraw Hill, Baltimore
-
Sapienza C, Hall JG (1995) Genome imprinting in human disease. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds) The metabolic basis of inherited disease, 7th ed. McGraw Hill, Baltimore, pp 437-458
-
(1995)
The Metabolic Basis of Inherited Disease, 7th Ed.
, pp. 437-458
-
-
Sapienza, C.1
Hall, J.G.2
-
39
-
-
0025641736
-
Premeiotic instability of repeated sequences in Neurospora crassa
-
Selker EU (1990) Premeiotic instability of repeated sequences in Neurospora crassa. Annu Rev Genet 24:579-613
-
(1990)
Annu Rev Genet
, vol.24
, pp. 579-613
-
-
Selker, E.U.1
-
40
-
-
0029056713
-
Deletion mapping of chromosome 11 in carcinoma of the bladder
-
Shaw ME, Knowles MA (1995) Deletion mapping of chromosome 11 in carcinoma of the bladder. Genes Chromosom Cancer 13:1-8
-
(1995)
Genes Chromosom Cancer
, vol.13
, pp. 1-8
-
-
Shaw, M.E.1
Knowles, M.A.2
-
42
-
-
0028356544
-
Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms tumor
-
Steenman MJC, Rainier S, Dobry CJ, Grundy P, Horon IL, Feinberg AP (1994) Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms tumor. Nat Genet 7:433-439
-
(1994)
Nat Genet
, vol.7
, pp. 433-439
-
-
Steenman, M.J.C.1
Rainier, S.2
Dobry, C.J.3
Grundy, P.4
Horon, I.L.5
Feinberg, A.P.6
-
43
-
-
0026922707
-
DNA methylation represses FMR-1 transcription in fragile X syndrome
-
Sutcliffe JS, Nelson DL, Zhang F, Pieretti M, Caskey CT, Saxe D, Warren ST (1992) DNA methylation represses FMR-1 transcription in fragile X syndrome. Hum Mol Genet 1: 397-400
-
(1992)
Hum Mol Genet
, vol.1
, pp. 397-400
-
-
Sutcliffe, J.S.1
Nelson, D.L.2
Zhang, F.3
Pieretti, M.4
Caskey, C.T.5
Saxe, D.6
Warren, S.T.7
-
44
-
-
0027189805
-
Loss of heterozygosity in malignant melanomas at loci on chromosomes 11 and 17 implicated in the pathogenesis of other cancers
-
Tomlinson IPM, Gammack AJ, Stickland JE, Mann GJ, MacKie RM, Kefford RF, McGee JOD (1993) Loss of heterozygosity in malignant melanomas at loci on chromosomes 11 and 17 implicated in the pathogenesis of other cancers. Genes Chromosom Cancer 7:169-172
-
(1993)
Genes Chromosom Cancer
, vol.7
, pp. 169-172
-
-
Tomlinson, I.P.M.1
Gammack, A.J.2
Stickland, J.E.3
Mann, G.J.4
MacKie, R.M.5
Kefford, R.F.6
McGee, J.O.D.7
-
45
-
-
0024404822
-
Genomic imprinting in hereditary glomus tumors: Evidence for new genetic theory
-
van der Mey AGL, Maaswinkel-Mooy PD, Cornelisse CJ, Schmidt PH, van de Kamp JJP (1989) Genomic imprinting in hereditary glomus tumors: evidence for new genetic theory. Lancet 2:1291-1294
-
(1989)
Lancet
, vol.2
, pp. 1291-1294
-
-
Van Der Mey, A.G.L.1
Maaswinkel-Mooy, P.D.2
Cornelisse, C.J.3
Schmidt, P.H.4
Van De Kamp, J.J.P.5
-
46
-
-
0024514647
-
Allelotype of colorectal carcinomas
-
Vogelstein B, Fearon ER, Kern SE, Hamilton SR, Preisinger AC, Nakamura Y, White R (1989) Allelotype of colorectal carcinomas. Science 244:207-211
-
(1989)
Science
, vol.244
, pp. 207-211
-
-
Vogelstein, B.1
Fearon, E.R.2
Kern, S.E.3
Hamilton, S.R.4
Preisinger, A.C.5
Nakamura, Y.6
White, R.7
|