-
1
-
-
18544405060
-
H19 overexpression in breast adenocarcinoma stromal cells is associated with tumor values and steroid receptor status but independent of p53 and Ki-67 expression
-
Adriaenssens E, Dumont L, Lottin S, Bolle D, Lepretre A, Delobelle A, Bouali F, Dugimont T, Coll J, Curgy JJ (1998) H19 overexpression in breast adenocarcinoma stromal cells is associated with tumor values and steroid receptor status but independent of p53 and Ki-67 expression. Am J Pathol 153:1597-1607
-
(1998)
Am J Pathol
, vol.153
, pp. 1597-1607
-
-
Adriaenssens, E.1
Dumont, L.2
Lottin, S.3
Bolle, D.4
Lepretre, A.5
Delobelle, A.6
Bouali, F.7
Dugimont, T.8
Coll, J.9
Curgy, J.J.10
-
2
-
-
0036351329
-
Cross-talk between mesenchyme and epithelium increases H19 gene expression during scattering and morphogenesis of epithelial cells
-
Adriaenssens E, Lottin S, Berteaux N, Hornez L, Fauquette W, Fafeur V, Peyrat JP, Le Bourhis X, Hondermarck H, Coll J, Dugimont T, Curgy JJ (2002) Cross-talk between mesenchyme and epithelium increases H19 gene expression during scattering and morphogenesis of epithelial cells. Exp Cell Res 275:215-229
-
(2002)
Exp Cell Res
, vol.275
, pp. 215-229
-
-
Adriaenssens, E.1
Lottin, S.2
Berteaux, N.3
Hornez, L.4
Fauquette, W.5
Fafeur, V.6
Peyrat, J.P.7
Le Bourhis, X.8
Hondermarck, H.9
Coll, J.10
Dugimont, T.11
Curgy, J.J.12
-
3
-
-
0033527067
-
Steroid hormones mdulate H19 gene expression in both mammary gland and uterus
-
Adriaenssens E, Lottin S, Dugimont T, Fauquette W, Coll J, Dupouy JP, Boilly B, Curgy JJ (1999) Steroid hormones mdulate H19 gene expression in both mammary gland and uterus. Oncogene 18:4460-4473
-
(1999)
Oncogene
, vol.18
, pp. 4460-4473
-
-
Adriaenssens, E.1
Lottin, S.2
Dugimont, T.3
Fauquette, W.4
Coll, J.5
Dupouy, J.P.6
Boilly, B.7
Curgy, J.J.8
-
4
-
-
0026063392
-
Hereditary gingival fibromatosis in a family with the Zimmermann-Laband syndrome
-
Bakaeen G, Scully C (1991) Hereditary gingival fibromatosis in a family with the Zimmermann-Laband syndrome. J Oral Pathol Med 20:457-459
-
(1991)
J Oral Pathol Med
, vol.20
, pp. 457-459
-
-
Bakaeen, G.1
Scully, C.2
-
5
-
-
0034602950
-
Mutations in SDHD, a mitochondrial complexII gene, in hereditary paraganglioma
-
Baysal BE, Ferrell RE, Willett-Brozick JE, Lawrence EC, Myssiorek D, Bosch A, van der Mey A, Taschner PE, Rubinstein WS, Myers EN, Richard CW 3rd, Cornelisse CJ, Devilee P, Devlin B (2000) Mutations in SDHD, a mitochondrial complexII gene, in hereditary paraganglioma. Science 287:848-851
-
(2000)
Science
, vol.287
, pp. 848-851
-
-
Baysal, B.E.1
Ferrell, R.E.2
Willett-Brozick, J.E.3
Lawrence, E.C.4
Myssiorek, D.5
Bosch, A.6
van der Mey, A.7
Taschner, P.E.8
Rubinstein, W.S.9
Myers, E.N.10
Richard III, C.W.11
Cornelisse, C.J.12
Devilee, P.13
Devlin, B.14
-
6
-
-
0034713375
-
Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene
-
Bell AC, Felsenfeld G (2000) Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene. Nature 405:482-485
-
(2000)
Nature
, vol.405
, pp. 482-485
-
-
Bell, A.C.1
Felsenfeld, G.2
-
7
-
-
0035910395
-
Insulators and boundaries: Versatile regulatory elements in the eukaryotic genome
-
Bell AC, West AG, Felsenfeld G (2001) Insulators and boundaries: versatile regulatory elements in the eukaryotic genome. Science 291:447-450
-
(2001)
Science
, vol.291
, pp. 447-450
-
-
Bell, A.C.1
West, A.G.2
Felsenfeld, G.3
-
9
-
-
0023909391
-
Hereditary generalized gingival fibromatosis associated with hypertrichosis: Report of five cases in one family
-
Cuestas-Carnero R, Bornancini CA (1988) Hereditary generalized gingival fibromatosis associated with hypertrichosis: Report of five cases in one family. J Oral Maxillofac Surg 46:415-420
-
(1988)
J Oral Maxillofac Surg
, vol.46
, pp. 415-420
-
-
Cuestas-Carnero, R.1
Bornancini, C.A.2
-
11
-
-
0033118754
-
Imprinting of a genomic domain of 11p15 and loss of imprinting in cancer: An introduction
-
Feinberg AP (1999) Imprinting of a genomic domain of 11p15 and loss of imprinting in cancer: An introduction. Cancer Res 59:1743-1746
-
(1999)
Cancer Res
, vol.59
, pp. 1743-1746
-
-
Feinberg, A.P.1
-
12
-
-
0036831864
-
Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1
-
Fitzpatrick GV, Soloway PD, Higgins MJ (2002) Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1. Nat Genet 32:426-431
-
(2002)
Nat Genet
, vol.32
, pp. 426-431
-
-
Fitzpatrick, G.V.1
Soloway, P.D.2
Higgins, M.J.3
-
13
-
-
0030348104
-
Gingival fibromatosis and partial duplication of the short arm of chromosome 2 (dup(2) (p13- > p21))
-
Fryns JP (1996) Gingival fibromatosis and partial duplication of the short arm of chromosome 2 (dup(2) (p13- > p21)). Ann Genet 39:54-55
-
(1996)
Ann Genet
, vol.39
, pp. 54-55
-
-
Fryns, J.P.1
-
14
-
-
0029300145
-
Gingival fibromatosis and Klippel-Trenaunay-Weber syndrome. Case report
-
Hallett KB, Bankier A, Chow CW, Bateman J, Hall RK (1995) Gingival fibromatosis and Klippel-Trenaunay-Weber syndrome. Case report. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 79:578-582
-
(1995)
Oral Surg Oral Med Oral Pathol Oral Radiol Endod
, vol.79
, pp. 578-582
-
-
Hallett, K.B.1
Bankier, A.2
Chow, C.W.3
Bateman, J.4
Hall, R.K.5
-
15
-
-
0027442239
-
Tumour-suppressor activity of H19 RNA
-
Hao Y, Crenshaw T, Moulton T, Newcomb E, Tycko B (1993) Tumour-suppressor activity of H19 RNA. Nature 365:764-767
-
(1993)
Nature
, vol.365
, pp. 764-767
-
-
Hao, Y.1
Crenshaw, T.2
Moulton, T.3
Newcomb, E.4
Tycko, B.5
-
16
-
-
0034713275
-
CTCF mediates methylation-sensitive enhancer-blocking activity at the H19 / Igf2 locus
-
Hark AT, Schoenherr CJ, Katz DJ, Ingram RS, Levorse JM, Tilghman SM (2000) CTCF mediates methylation-sensitive enhancer-blocking activity at the H19 / Igf2 locus. Nature 405:486-489
-
(2000)
Nature
, vol.405
, pp. 486-489
-
-
Hark, A.T.1
Schoenherr, C.J.2
Katz, D.J.3
Ingram, R.S.4
Levorse, J.M.5
Tilghman, S.M.6
-
17
-
-
0031946852
-
Genetic linkage of hereditary gingival fibromatosis to chromosome 2p21
-
Hart TC, Pallos D, Bowden DW, Bolyard J, Pettenati MJ, Cortelli JR (1998) Genetic linkage of hereditary gingival fibromatosis to chromosome 2p21. Am J Hum Genet 62:876-883
-
(1998)
Am J Hum Genet
, vol.62
, pp. 876-883
-
-
Hart, T.C.1
Pallos, D.2
Bowden, D.W.3
Bolyard, J.4
Pettenati, M.J.5
Cortelli, J.R.6
-
18
-
-
0034441673
-
Evidence of genetic heterogeneity for hereditary gingival fibromatosis
-
Hart TC, Pallos D, Bozzo L, Almeida OP, Marazita ML, O'Connell JR, Cortelli JR (2000) Evidence of genetic heterogeneity for hereditary gingival fibromatosis. J Dent Res 79:1758-1764
-
(2000)
J Dent Res
, vol.79
, pp. 1758-1764
-
-
Hart, T.C.1
Pallos, D.2
Bozzo, L.3
Almeida, O.P.4
Marazita, M.L.5
O'Connell, J.R.6
Cortelli, J.R.7
-
19
-
-
0036201303
-
A mutation in the SOS1 gene causes hereditary gingival fibromatosis type1
-
Hart TC, Zhang Y, Gorry MC, Hart PS, Cooper M, Marazita ML, Marks JM, Cortelli JR, Pallos D (2002) A mutation in the SOS1 gene causes hereditary gingival fibromatosis type1. Am J Hum Genet 70:943-954
-
(2002)
Am J Hum Genet
, vol.70
, pp. 943-954
-
-
Hart, T.C.1
Zhang, Y.2
Gorry, M.C.3
Hart, P.S.4
Cooper, M.5
Marazita, M.L.6
Marks, J.M.7
Cortelli, J.R.8
Pallos, D.9
-
20
-
-
0025829628
-
Drug-induced gingival overgrowth: Old problem, new problem
-
Hassell TM, Hefti AF (1991) Drug-induced gingival overgrowth: Old problem, new problem. Crit Rev Oral Biol Med 2:103-137
-
(1991)
Crit Rev Oral Biol Med
, vol.2
, pp. 103-137
-
-
Hassell, T.M.1
Hefti, A.F.2
-
21
-
-
0024514494
-
Tumor-specific loss of 11p15.5 alleles in del11p13 wilms tumor and in familial adrenocortical carcinoma
-
Henry I, Grandjouan S, Couillin P, Barichard F, Huerre-Jeanpierre C, Glaser T, Philip T, Lenoir G, Chaussain JL, Junien C (1989) Tumor-specific loss of 11p15.5 alleles in del11p13 wilms tumor and in familial adrenocortical carcinoma. Proc Natl Acad Sci USA 86:3247-3251
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 3247-3251
-
-
Henry, I.1
Grandjouan, S.2
Couillin, P.3
Barichard, F.4
Huerre-Jeanpierre, C.5
Glaser, T.6
Philip, T.7
Lenoir, G.8
Chaussain, J.L.9
Junien, C.10
-
22
-
-
2942561954
-
Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma families
-
Hensen EF, Jordanova ES, van Minderhout IJ, Hogendoorn PC, Taschner PE, van der Mey AG, Devilee P, Cornelisse CJ (2004) Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma families. Oncogene 23:4076-4083
-
(2004)
Oncogene
, vol.23
, pp. 4076-4083
-
-
Hensen, E.F.1
Jordanova, E.S.2
van Minderhout, I.J.3
Hogendoorn, P.C.4
Taschner, P.E.5
van der Mey, A.G.6
Devilee, P.7
Cornelisse, C.J.8
-
23
-
-
0034284693
-
Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome
-
Horike S, Mitsuya K, Meguro M, Kotobuki N, Kashiwagi A, Notsu T, Schulz TC, Shirayoshi Y, Oshimura M (2000) Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome. Hum Mol Genet 9:2075-2083
-
(2000)
Hum Mol Genet
, vol.9
, pp. 2075-2083
-
-
Horike, S.1
Mitsuya, K.2
Meguro, M.3
Kotobuki, N.4
Kashiwagi, A.5
Notsu, T.6
Schulz, T.C.7
Shirayoshi, Y.8
Oshimura, M.9
-
24
-
-
0016193707
-
Variation in the inheritance and expression of gingival fibromatosis
-
M.E
-
Jorgenson RJC, M.E. (1974) Variation in the inheritance and expression of gingival fibromatosis. J Periodontol 45:472-477
-
(1974)
J Periodontol
, vol.45
, pp. 472-477
-
-
Jorgenson, R.J.C.1
-
25
-
-
0031945309
-
Two distinct tumor suppressor loci within chromosome 11p15 implicated in breast cancer progression and metastasis
-
Karnik P, Paris M, Williams BR, Casey G, Crowe J, Chen P (1998) Two distinct tumor suppressor loci within chromosome 11p15 implicated in breast cancer progression and metastasis. Hum Mol Genet 7:895-903
-
(1998)
Hum Mol Genet
, vol.7
, pp. 895-903
-
-
Karnik, P.1
Paris, M.2
Williams, B.R.3
Casey, G.4
Crowe, J.5
Chen, P.6
-
26
-
-
0034853634
-
Frequent loss of imprinting of IGF2 and MEST in lung adenocarcinoma
-
Kohda M, Hoshiya H, Katoh M, Tanaka I, Masuda R, Takemura T, Fujiwara M, Oshimura M (2001) Frequent loss of imprinting of IGF2 and MEST in lung adenocarcinoma. Mol Carcinog 31:184-191
-
(2001)
Mol Carcinog
, vol.31
, pp. 184-191
-
-
Kohda, M.1
Hoshiya, H.2
Katoh, M.3
Tanaka, I.4
Masuda, R.5
Takemura, T.6
Fujiwara, M.7
Oshimura, M.8
-
27
-
-
0027231784
-
Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from chromosome 11
-
Koi M, Johnson LA, Kalikin LM, Little PF, 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.4
Nakamura, Y.5
Feinberg, A.P.6
-
28
-
-
0028905376
-
Frequent loss of imprinting of the H19 gene is often associated with its overexpression in human lung cancers
-
Kondo M, Suzuki H, Ueda R, Osada H, Takagi K, Takahashi T, Takahashi T (1995) Frequent loss of imprinting of the H19 gene is often associated with its overexpression in human lung cancers. Oncogene 10:1193-1198
-
(1995)
Oncogene
, vol.10
, pp. 1193-1198
-
-
Kondo, M.1
Suzuki, H.2
Ueda, R.3
Osada, H.4
Takagi, K.5
Takahashi, T.6
Takahashi, T.7
-
29
-
-
0000547204
-
Hereditary gingival fibromatosis. Report of an affected family with associated splenomegaly and skeletal and soft-tissue abnormalities
-
Laband PF, Habib G, Humphreys GS (1964) Hereditary gingival fibromatosis. Report of an affected family with associated splenomegaly and skeletal and soft-tissue abnormalities. Oral Surg Oral Med Oral Pathol 17:339-351
-
(1964)
Oral Surg Oral Med Oral Pathol
, vol.17
, pp. 339-351
-
-
Laband, P.F.1
Habib, G.2
Humphreys, G.S.3
-
31
-
-
11144330666
-
The human H19 gene is frequently overexpressed in myometrium and stroma during pathological endometrial proliferative events
-
Lottin S, Adriaenssens E, Berteaux N, Lepretre A, Vilain MO, Denhez E, Coll J, Dugimont T, Curgy JJ (2005) The human H19 gene is frequently overexpressed in myometrium and stroma during pathological endometrial proliferative events. Eur J Cancer 41:168-177
-
(2005)
Eur J Cancer
, vol.41
, pp. 168-177
-
-
Lottin, S.1
Adriaenssens, E.2
Berteaux, N.3
Lepretre, A.4
Vilain, M.O.5
Denhez, E.6
Coll, J.7
Dugimont, T.8
Curgy, J.J.9
-
32
-
-
0036849920
-
Overexpression of an ectopic H19 gene enhances the tumorigenic properties of breast cancer cells
-
Lottin S, Adriaenssens E, Dupressoir T, Berteaux N, Montpellier C, Coll J, Dugimont T, Curgy JJ (2002) Overexpression of an ectopic H19 gene enhances the tumorigenic properties of breast cancer cells. Carcinogenesis 23:1885-1895
-
(2002)
Carcinogenesis
, vol.23
, pp. 1885-1895
-
-
Lottin, S.1
Adriaenssens, E.2
Dupressoir, T.3
Berteaux, N.4
Montpellier, C.5
Coll, J.6
Dugimont, T.7
Curgy, J.J.8
-
33
-
-
0028988159
-
CDKN1C, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene
-
Matsuoka S, Edwards MC, Bai C, Parker S, Zhang P, Baldini A, Harper JW, Elledge SJ (1995) CDKN1C, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene. Genes Dev 9:650-662
-
(1995)
Genes Dev
, vol.9
, pp. 650-662
-
-
Matsuoka, S.1
Edwards, M.C.2
Bai, C.3
Parker, S.4
Zhang, P.5
Baldini, A.6
Harper, J.W.7
Elledge, S.J.8
-
34
-
-
0025099414
-
Ectro-amelia syndrome associated with an interstitial deletion of 7q
-
Morey MA, Higgins RR (1990) Ectro-amelia syndrome associated with an interstitial deletion of 7q. Am J Med Genet 35:95-99
-
(1990)
Am J Med Genet
, vol.35
, pp. 95-99
-
-
Morey, M.A.1
Higgins, R.R.2
-
35
-
-
0031279892
-
The pre-implantation ontogeny of the H19 methylation imprint
-
Olek A, Walter J (1997) The pre-implantation ontogeny of the H19 methylation imprint. Nat Genet 17:275-276
-
(1997)
Nat Genet
, vol.17
, pp. 275-276
-
-
Olek, A.1
Walter, J.2
-
36
-
-
22044445705
-
Decreased expression of haemoglobin beta (HBB) gene in anaplastic thyroid cancer and recovery of its expression inhibits cell growth
-
Onda M, Akaishi J, Asaka S, Okamoto J, Miyamoto S, Mizutani K, Yoshida A, Ito K, Emi M (2005) Decreased expression of haemoglobin beta (HBB) gene in anaplastic thyroid cancer and recovery of its expression inhibits cell growth. Br J Cancer 92:2216-2224
-
(2005)
Br J Cancer
, vol.92
, pp. 2216-2224
-
-
Onda, M.1
Akaishi, J.2
Asaka, S.3
Okamoto, J.4
Miyamoto, S.5
Mizutani, K.6
Yoshida, A.7
Ito, K.8
Emi, M.9
-
37
-
-
84984486092
-
Hereditary fibrous hyperplasia of the gingiva with varying penetrance and expressivity
-
Raeste AM, Collan Y, Kilpinen E (1978) Hereditary fibrous hyperplasia of the gingiva with varying penetrance and expressivity. Scand J Dent Res 86:357-365
-
(1978)
Scand J Dent Res
, vol.86
, pp. 357-365
-
-
Raeste, A.M.1
Collan, Y.2
Kilpinen, E.3
-
38
-
-
0027172683
-
Relaxation of imprinted genes in human cancer
-
Rainier S, Johnson LA, Dobry CJ, Ping AJ, Grundy PE, Feinberg AP (1993) Relaxation of imprinted genes in human cancer. Nature 362:747-749
-
(1993)
Nature
, vol.362
, pp. 747-749
-
-
Rainier, S.1
Johnson, L.A.2
Dobry, C.J.3
Ping, A.J.4
Grundy, P.E.5
Feinberg, A.P.6
-
39
-
-
0035234557
-
Genomic imprinting: Parental influence on the genome
-
Reik W, Walter J (2001) Genomic imprinting: Parental influence on the genome. Nat Rev Genet 2:21-32
-
(2001)
Nat Rev Genet
, vol.2
, pp. 21-32
-
-
Reik, W.1
Walter, J.2
-
40
-
-
0026673534
-
Opposite imbalances of distal 14q in two unrelated patients
-
Rivera H, Ramirez-Duenas ML, Figuera LE, Gonzalez-Montes RM, Vasquez AI (1992) Opposite imbalances of distal 14q in two unrelated patients. Ann Genet 35:97-100
-
(1992)
Ann Genet
, vol.35
, pp. 97-100
-
-
Rivera, H.1
Ramirez-Duenas, M.L.2
Figuera, L.E.3
Gonzalez-Montes, R.M.4
Vasquez, A.I.5
-
41
-
-
20144374299
-
Loss of imprinting of Igf2 alters intestinal maturation and tumorigenesis in mice
-
Sakatani T, Kaneda A, Iacobuzio-Donahue CA, Carter MG, de Boom Witzel S, Okano H, Ko MS, Ohlsson R, Longo DL, Feinberg AP (2005) Loss of imprinting of Igf2 alters intestinal maturation and tumorigenesis in mice. Science 307:1976-1978
-
(2005)
Science
, vol.307
, pp. 1976-1978
-
-
Sakatani, T.1
Kaneda, A.2
Iacobuzio-Donahue, C.A.3
Carter, M.G.4
de Boom Witzel, S.5
Okano, H.6
Ko, M.S.7
Ohlsson, R.8
Longo, D.L.9
Feinberg, A.P.10
-
42
-
-
0027755783
-
Hereditary gingival fibromatosis with a recessive mode of inheritance. Case reports
-
Singer SL, Goldblatt J, Hallam LA, Winters JC (1993) Hereditary gingival fibromatosis with a recessive mode of inheritance. Case reports. Aust Dent J 38:427-432
-
(1993)
Aust Dent J
, vol.38
, pp. 427-432
-
-
Singer, S.L.1
Goldblatt, J.2
Hallam, L.A.3
Winters, J.C.4
-
43
-
-
0033529207
-
A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome
-
Smilinich NJ, Day CD, Fitzpatrick GV, Caldwell GM, Lossie AC, Cooper PR, Smallwood AC, Joyce JA, Schofield PN, Reik W, Nicholls RD, Weksberg R, Driscoll DJ, Maher ER, Shows TB, Higgins MJ (1999) A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome. Proc Natl Acad Sci USA 96:8064-8069
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 8064-8069
-
-
Smilinich, N.J.1
Day, C.D.2
Fitzpatrick, G.V.3
Caldwell, G.M.4
Lossie, A.C.5
Cooper, P.R.6
Smallwood, A.C.7
Joyce, J.A.8
Schofield, P.N.9
Reik, W.10
Nicholls, R.D.11
Weksberg, R.12
Driscoll, D.J.13
Maher, E.R.14
Shows, T.B.15
Higgins, M.J.16
-
44
-
-
0029945706
-
Descent graphs in pedigree analysis: Applications to haplotyping, location scores, and marker-sharing statistics
-
Sobel E, Lange K (1996) Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics. Am J Hum Genet 58:1323-1337
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1323-1337
-
-
Sobel, E.1
Lange, K.2
-
45
-
-
0027424663
-
Natural history of the recombinant (eight) syndrome
-
Sujansky E, Smith AC, Prescott KE, Freehauf CL, Clericuzio C, Robinson A (1993) Natural history of the recombinant (eight) syndrome. Am J Med Genet 47:512-525
-
(1993)
Am J Med Genet
, vol.47
, pp. 512-525
-
-
Sujansky, E.1
Smith, A.C.2
Prescott, K.E.3
Freehauf, C.L.4
Clericuzio, C.5
Robinson, A.6
-
46
-
-
0032419812
-
Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2
-
Thorvaldsen JL, Duran KL, Bartolomei MS (1998) Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2. Genes Dev 12:3693-3702
-
(1998)
Genes Dev
, vol.12
, pp. 3693-3702
-
-
Thorvaldsen, J.L.1
Duran, K.L.2
Bartolomei, M.S.3
-
47
-
-
0015068755
-
Heterogeneity in gingival fibromatosis
-
Witkop CJ Jr (1971) Heterogeneity in gingival fibromatosis. Birth Defects Orig Artic Ser 7:210-221
-
(1971)
Birth Defects Orig Artic Ser
, vol.7
, pp. 210-221
-
-
Witkop Jr, C.J.1
-
48
-
-
0028370014
-
H19, a tumour suppressing RNA?
-
Wrana JL (1994) H19, a tumour suppressing RNA? Bioessays 16:89-90
-
(1994)
Bioessays
, vol.16
, pp. 89-90
-
-
Wrana, J.L.1
-
49
-
-
0035367868
-
A new locus for hereditary gingival fibromatosis (GINGF2) maps to 5q13-q22
-
Xiao S, Bu L, Zhu L, Zheng G, Yang M, Qian M, Hu L, Liu J, Zhao G, Kong X (2001) A new locus for hereditary gingival fibromatosis (GINGF2) maps to 5q13-q22. Genomics 74:180-185
-
(2001)
Genomics
, vol.74
, pp. 180-185
-
-
Xiao, S.1
Bu, L.2
Zhu, L.3
Zheng, G.4
Yang, M.5
Qian, M.6
Hu, L.7
Liu, J.8
Zhao, G.9
Kong, X.10
-
50
-
-
0034665198
-
Refinement of the locus for autosomal dominant hereditary gingival fibromatosis (GINGF) to a 3.8-cM region on 2p21
-
Xiao S, Wang X, Qu B, Yang M, Liu G, Bu L, Wang Y, Zhu L, Lei H, Hu L, Zhang X, Liu J, Zhao G, Kong X (2000) Refinement of the locus for autosomal dominant hereditary gingival fibromatosis (GINGF) to a 3.8-cM region on 2p21. Genomics 68:247-252
-
(2000)
Genomics
, vol.68
, pp. 247-252
-
-
Xiao, S.1
Wang, X.2
Qu, B.3
Yang, M.4
Liu, G.5
Bu, L.6
Wang, Y.7
Zhu, L.8
Lei, H.9
Hu, L.10
Zhang, X.11
Liu, J.12
Zhao, G.13
Kong, X.14
-
51
-
-
23844483676
-
A novel locus for autosomal dominant hereditary gingival fibromatosis, GINGF3, maps to chromosome 2p22.3-p23.3
-
Ye X, Shi L, Cheng Y, Peng Q, Huang S, Liu J, Huang M, Peng B, Bian Z (2005) A novel locus for autosomal dominant hereditary gingival fibromatosis, GINGF3, maps to chromosome 2p22.3-p23.3. Clin Genet 68:239-244
-
(2005)
Clin Genet
, vol.68
, pp. 239-244
-
-
Ye, X.1
Shi, L.2
Cheng, Y.3
Peng, Q.4
Huang, S.5
Liu, J.6
Huang, M.7
Peng, B.8
Bian, Z.9
-
52
-
-
0024590839
-
A terminal deletion (14)(q31.1) in a child with microcephaly, narrow palate, gingival hypertrophy, protuberant ears, and mild mental retardation
-
Yen FS, Podruch PE, Weisskopf B (1989) A terminal deletion (14)(q31.1) in a child with microcephaly, narrow palate, gingival hypertrophy, protuberant ears, and mild mental retardation. J Med Genet 26:130-133
-
(1989)
J Med Genet
, vol.26
, pp. 130-133
-
-
Yen, F.S.1
Podruch, P.E.2
Weisskopf, B.3
|