-
1
-
-
0028909493
-
Deletion mapping of the long arm of chromosome 22 in human meningiomas
-
1 Akagi K, Kurahashi H, Arita N et al. Deletion mapping of the long arm of chromosome 22 in human meningiomas. Int J Cancer 1995 ; 60: 178–82.
-
(1995)
Int J Cancer
, vol.60
, pp. 178-82
-
-
Akagi, K1
Kurahashi, H2
Arita, N3
-
2
-
-
0022578671
-
Multifocal meningiomas in a patient with a constitutional ring chromosome 2
-
2 Arinami T, Kondo I, Hamaguchi H, Nakajima S. Multifocal meningiomas in a patient with a constitutional ring chromosome 2. Med Genet 1986 ; 23: 178–80.
-
(1986)
Med Genet
, vol.23
, pp. 178-80
-
-
Arinami, T1
Kondo, I2
Hamaguchi, H3
Nakajima, S.4
-
3
-
-
0026443054
-
Molecular characterization of chromosome 22 in schwannomas
-
3 Bijlsma EK, Brouwer‐Mladin R, Bosch DA, Westerveld A, Hulsebos TJM. Molecular characterization of chromosome 22 in schwannomas. Genes Chrom Cancer 1992 ; 5: 201–5.
-
(1992)
Genes Chrom Cancer
, vol.5
, pp. 201-5
-
-
Bijlsma, EK1
Brouwer‐Mladin, R2
Bosch, DA3
Westerveld, A4
Hulsebos, TJM.5
-
4
-
-
0028226739
-
Germline mutations in the neurofibromatosis type two tumour suppressor gene
-
4 Bourn D, Carter SA, Mason S, Evans DGR, Strachan T. Germline mutations in the neurofibromatosis type two tumour suppressor gene. Hum Mol Genet 1994 ; 3: 813–6.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 813-6
-
-
Bourn, D1
Carter, SA2
Mason, S3
Evans, DGR4
Strachan, T.5
-
5
-
-
0029061177
-
Translocation (12; 22) (p. 13; q11) in myeloproliferative disorders results in fusion of the ETS‐like TEL gene on 12p13 to the MM1 gene on 22q11
-
5 Buijs A, Sherr S, Van Baal S et al. Translocation (12; 22) (p. 13; q11) in myeloproliferative disorders results in fusion of the ETS‐like TEL gene on 12p13 to the MM1 gene on 22q11. Oncogene 1995 ; 10: 1511–9.
-
(1995)
Oncogene
, vol.10
, pp. 1511-9
-
-
Buijs, A1
Sherr, S2
Van Baal, S3
-
6
-
-
0029653651
-
A high density yeast artificial chromosome contig map of human chromosome 22
-
6 Collins JE, Cole CG, Smink LJ, Garrett CL, Leversha MA, Soderlund CA. A high density yeast artificial chromosome contig map of human chromosome 22. Nature 1995 ; 377: 367–79.
-
(1995)
Nature
, vol.377
, pp. 367-79
-
-
Collins, JE1
Cole, CG2
Smink, LJ3
Garrett, CL4
Leversha, MA5
Soderlund, CA.6
-
7
-
-
0025832422
-
Allelotype of human breast carcinoma; a second major site for loss of heterozygozity is on chromosome 6q
-
7 Devilee P et al. Allelotype of human breast carcinoma; a second major site for loss of heterozygozity is on chromosome 6q. Oncogene 1991 ; 6: 1705–11.
-
(1991)
Oncogene
, vol.6
, pp. 1705-11
-
-
Devilee, P1
-
8
-
-
0013556122
-
Deletion mapping of a locus on human chromosome 22 involved in the oncogenesis of meningioma
-
8 Dumanski JP, Carlbom E, Collins VP, Nordenskjöld M. Deletion mapping of a locus on human chromosome 22 involved in the oncogenesis of meningioma. Proc Natl Acad Sci USA 1987 ; 84: 9275–9.
-
(1987)
Proc Natl Acad Sci USA
, vol.84
, pp. 9275-9
-
-
Dumanski, JP1
Carlbom, E2
Collins, VP3
Nordenskjöld, M.4
-
9
-
-
0019761388
-
Central neurofibromatosis with bilateral acoustic neuroma, in: Neurofibromatosis (Von Recklinghausen Disease); Genetics, Cell Biology and Biochemistry
-
9 Eldridge R. Central neurofibromatosis with bilateral acoustic neuroma. In: Neurofibromatosis (Von Recklinghausen Disease); Genetics, Cell Biology and Biochemistry, Riccardi VM, Mulvihill JJ, Eds. New York: Raven Press, 1981: 57–65. Advances in Neurology; Vol. 29.
-
(1981)
, vol.29
, pp. 57-65
-
-
Eldridge, R.1
-
10
-
-
0005282010
-
Neurofibromatosis 2: clinical heterogeneity and natural history in 39 individuals in nine families and 16 sporadic cases
-
10 Eldridge R, Parry DM, Kaiser‐Kupfer MI. Neurofibromatosis 2: clinical heterogeneity and natural history in 39 individuals in nine families and 16 sporadic cases. Am J Hum Gen 1991 ; 49: 32.
-
(1991)
Am J Hum Gen
, vol.49
, pp. 32
-
-
Eldridge, R1
Parry, DM2
Kaiser‐Kupfer, MI.3
-
11
-
-
11944267671
-
A genetic study of type two neurofibromatosis in the United Kingdom. I. Prevalence, mutation rate, fitness, and confirmation of maternal transmission effect on severity. J
-
11 Evans DGR, Huson SM, Donnai D et al. A genetic study of type two neurofibromatosis in the United Kingdom. I. Prevalence, mutation rate, fitness, and confirmation of maternal transmission effect on severity. J. Med Genet 1992 ; 29: 841–6.
-
(1992)
Med Genet
, vol.29
, pp. 841-6
-
-
Evans, DGR1
Huson, SM2
Donnai, D3
-
12
-
-
0027080030
-
A genetic study of type two neurofibromatosis in the United Kingdom. II. Guidelines for genetic counseling
-
12 Evans DGR, Huson SM, Donnai D et al. A genetic study of type two neurofibromatosis in the United Kingdom. II. Guidelines for genetic counseling. J. Med Genet 1992 ; 29: 847–52.
-
(1992)
J. Med Genet
, vol.29
, pp. 847-52
-
-
Evans, DGR1
Huson, SM2
Donnai, D3
-
13
-
-
0026746684
-
A clinical study of type two neurofibromatosis
-
13 Evans DGR, Huson M, Donnai D et al. A clinical study of type two neurofibromatosis. Q J Med 1992 ; 84: 603–18.
-
(1992)
Q J Med
, vol.84
, pp. 603-18
-
-
Evans, DGR1
Huson, M2
Donnai, D3
-
14
-
-
0025143557
-
Loss of genetic information in central nervous system tumors common to children and young adults
-
14 James CD, He J, Carlbom E et al. Loss of genetic information in central nervous system tumors common to children and young adults. Genes Chrom Cancer 1990 ; 2: 94–102.
-
(1990)
Genes Chrom Cancer
, vol.2
, pp. 94-102
-
-
James, CD1
He, J2
Carlbom, E3
-
15
-
-
0018821706
-
Central neurofibromatosis with bilateral acoustic neuroma: genetic, clinical and biochemical distinctions from peripheral neurofibromatosis
-
15 Kanter WR, Eldridge R, Fabricant R, Allen JC, Koerber T. Central neurofibromatosis with bilateral acoustic neuroma: genetic, clinical and biochemical distinctions from peripheral neurofibromatosis. Neurology 1980 ; 30: 851–9.
-
(1980)
Neurology
, vol.30
, pp. 851-9
-
-
Kanter, WR1
Eldridge, R2
Fabricant, R3
Allen, JC4
Koerber, T.5
-
16
-
-
0024404739
-
Report of the committee on the genetic constitution of chromosome 22
-
16 Kaplan J‐C, Emanuel BS. Report of the committee on the genetic constitution of chromosome 22. Cytogenet Cell Genet 1989 ; 51: 372–83.
-
(1989)
Cytogenet Cell Genet
, vol.51
, pp. 372-83
-
-
Kaplan, J‐C1
Emanuel, BS.2
-
17
-
-
0029102665
-
Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11
-
17 Karayiorgou M, Morris MA, Morrow B et al. Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11. Proc Natl Acad Sci USA 1995 ; 92: 7612–16.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 7612-16
-
-
Karayiorgou, M1
Morris, MA2
Morrow, B3
-
18
-
-
0004027454
-
Meningiomas: Biology, Pathology and Differential Diagnosis
-
18 Kepes JJ. Meningiomas: Biology, Pathology and Differential Diagnosis. New York: Masson Publishing, Inc. USA, 1982.
-
(1982)
-
-
Kepes, JJ.1
-
19
-
-
0025066085
-
Genomic alterations in human breast carcinomas
-
19 Larsson C, Byström C, Skoog L, Rotstein S, Nordenskjöld M. Genomic alterations in human breast carcinomas. Genes Chrom Cancer 1990 ; 2: 191–7.
-
(1990)
Genes Chrom Cancer
, vol.2
, pp. 191-7
-
-
Larsson, C1
Byström, C2
Skoog, L3
Rotstein, S4
Nordenskjöld, M.5
-
20
-
-
0028140423
-
Constitutional DNA‐level aberrations in chromosome 22 in a patient with multiple meningiomas
-
20 Lekanne Deprez RH, Groen NA, Louz D et al. Constitutional DNA‐level aberrations in chromosome 22 in a patient with multiple meningiomas. Genes Chrom Cancer 1994 ; 9: 124–8.
-
(1994)
Genes Chrom Cancer
, vol.9
, pp. 124-8
-
-
Lekanne, Deprez RH1
Groen, NA2
Louz, D3
-
21
-
-
0011790148
-
Frequent NF2 gene transcript mutations in sporadic meningiomas and vestibular schwannomas
-
21 Lekanne Deprez RH, Bianchi AB, Groen NA et al. Frequent NF2 gene transcript mutations in sporadic meningiomas and vestibular schwannomas. Am J Hum Genet 1994 ; 54: 1022–9.
-
(1994)
Am J Hum Genet
, vol.54
, pp. 1022-9
-
-
Lekanne, Deprez RH1
Bianchi, AB2
Groen, NA3
-
22
-
-
0029026395
-
Cloning and characterization of MN1, a gene from chromosome 22q11 which is disrupted by a balanced translocation in a meningioma
-
22 Lekanne Deprez RH, Riegman PHJ, Groen NA et al. Cloning and characterization of MN1, a gene from chromosome 22q11 which is disrupted by a balanced translocation in a meningioma. Oncogene 1995 ; 10: 1521–8.
-
(1995)
Oncogene
, vol.10
, pp. 1521-8
-
-
Lekanne, Deprez RH1
Riegman, PHJ2
Groen, NA3
-
23
-
-
0028932401
-
Cytogenetic, molecular genetic and pathological analyses in 126 meningiomas
-
23 Lekanne Deprez RH, Riegman PH, Van Drunen E et al. Cytogenetic, molecular genetic and pathological analyses in 126 meningiomas. J. Neuropathol Exp Neurol 1995 ; 54: 224–35.
-
(1995)
J. Neuropathol Exp Neurol
, vol.54
, pp. 224-35
-
-
Lekanne, Deprez RH1
Riegman, PH2
Van Drunen, E3
-
24
-
-
0028348101
-
Chromosomal deletions in anaplastic meningiomas suggest mutiple regions outside chromosome 22 as important for the tumour development and progression
-
24 Lindblom A, Ruttledge M, Collins VP, Nordenskjöld M, Dumanski JP. Chromosomal deletions in anaplastic meningiomas suggest mutiple regions outside chromosome 22 as important for the tumour development and progression. Int J Cancer 1994 ; 56: 354–7.
-
(1994)
Int J Cancer
, vol.56
, pp. 354-7
-
-
Lindblom, A1
Ruttledge, M2
Collins, VP3
Nordenskjöld, M4
Dumanski, JP.5
-
25
-
-
0028328785
-
Predisposition for breast cancer in carriers of constitutional translocation 11q; 22q
-
25 Lindblom A, Sandelin K, Iselius L et al. Predisposition for breast cancer in carriers of constitutional translocation 11q; 22q. Am J Hum Genet 1994 ; 54: 871–6.
-
(1994)
Am J Hum Genet
, vol.54
, pp. 871-6
-
-
Lindblom, A1
Sandelin, K2
Iselius, L3
-
26
-
-
0027359586
-
DNA diagnosis of neurofibromatosis 2
-
26 MacCollin MM, Mohney T, Trofatter JA, Wertelecki W, Ramesh V, Gusella JF. DNA diagnosis of neurofibromatosis 2. JAMA 1993 ; 270: 2316–20.
-
(1993)
JAMA
, vol.270
, pp. 2316-20
-
-
MacCollin, MM1
Mohney, T2
Trofatter, JA3
Wertelecki, W4
Ramesh, V5
Gusella, JF.6
-
27
-
-
0023597512
-
Loss of heterozygozity and the origin of meningioma
-
27 Meese E, Blin N, Zang KD. Loss of heterozygozity and the origin of meningioma. Hum Genet 1987 ; 77: 349–51.
-
(1987)
Hum Genet
, vol.77
, pp. 349-51
-
-
Meese, E1
Blin, N2
Zang, KD.3
-
28
-
-
0028837397
-
Screening for germ line mutations in the NF2 gene
-
28 Merel P, Hoang‐Xuan K, Sanson M et al. Screening for germ line mutations in the NF2 gene. Genes Chrom Cancer 1995 ; 12: 117–27.
-
(1995)
Genes Chrom Cancer
, vol.12
, pp. 117-27
-
-
Merel, P1
Hoang‐Xuan, K2
Sanson, M3
-
29
-
-
0029004033
-
Predominant occurrence of somatic mutations of the NF2 gene in meningiomas and schwannomas
-
29 Merel P, Hoang‐Xuan K, Sanson M et al. Predominant occurrence of somatic mutations of the NF2 gene in meningiomas and schwannomas. Genes Chrom Cancer 1995 ; 13: 211–6.
-
(1995)
Genes Chrom Cancer
, vol.13
, pp. 211-6
-
-
Merel, P1
Hoang‐Xuan, K2
Sanson, M3
-
30
-
-
0028053136
-
Clinical, cytogenetic and molecular characterization of seven patients with deletions of chromosome 22q13.3
-
30 Nesslinger N, GorsKi JL, Kurczynski TW et al. Clinical, cytogenetic and molecular characterization of seven patients with deletions of chromosome 22q13.3. Am J Hum Genet 1994 ; 54: 464–72.
-
(1994)
Am J Hum Genet
, vol.54
, pp. 464-72
-
-
Nesslinger, N1
GorsKi, JL2
Kurczynski, TW3
-
31
-
-
0023858742
-
Loss of constitutional heterozygozity in colon carcinoma from patients with familial polyposis coli
-
31 Okamoto M, Sasaki M, Sugio K et al. Loss of constitutional heterozygozity in colon carcinoma from patients with familial polyposis coli. Nature 1988 ; 331: 273–7.
-
(1988)
Nature
, vol.331
, pp. 273-7
-
-
Okamoto, M1
Sasaki, M2
Sugio, K3
-
32
-
-
0029006919
-
Ring chromosomes in dermatofibrosarcoma protuberans are low‐level amplifiers of chromosome 17 and 22 sequences
-
32 Pedeutour F, Simon M‐P, Minoletti F et al. Ring chromosomes in dermatofibrosarcoma protuberans are low‐level amplifiers of chromosome 17 and 22 sequences. Cancer Res 1995 ; 55: 2400–3.
-
(1995)
Cancer Res
, vol.55
, pp. 2400-3
-
-
Pedeutour, F1
Simon, M‐P2
Minoletti, F3
-
33
-
-
0027250547
-
Multiple meningiomas in a patient with constitutional ring chromosome 22
-
33 Petrella R, Lewine S, Wilmot PL, Ashar KD, Casamassima AC, Shapiro LR. Multiple meningiomas in a patient with constitutional ring chromosome 22. Am J Med Genet 1993 ; 47: 184–6.
-
(1993)
Am J Med Genet
, vol.47
, pp. 184-6
-
-
Petrella, R1
Lewine, S2
Wilmot, PL3
Ashar, KD4
Casamassima, AC5
Shapiro, LR.6
-
34
-
-
0028074376
-
Characterization of a new member of the human β‐adaptin gene family from chromosome 22q12, a candidate meningioma gene
-
34 Peyrard M, Fransson I, Xie Y‐G et al. Characterization of a new member of the human β‐adaptin gene family from chromosome 22q12, a candidate meningioma gene. Hum Mol Genet 1994 ; 3: 1393–9.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1393-9
-
-
Peyrard, M1
Fransson, I2
Xie, Y‐G3
-
35
-
-
0028082293
-
Sequential strategy to identify a susceptibility gene for schizophrenia: report of potential linkage on chromosome 22q12–q13.1
-
35 Pulver AE, Karayiorgou M, Wolyniec PS. Sequential strategy to identify a susceptibility gene for schizophrenia: report of potential linkage on chromosome 22q12–q13.1. Am J Med Genet (Neuropsych Genet) 1994 ; 54: 36–43.
-
(1994)
Am J Med Genet (Neuropsych Genet)
, vol.54
, pp. 36-43
-
-
Pulver, AE1
Karayiorgou, M2
Wolyniec, PS.3
-
36
-
-
0023813719
-
Chromosomal involvement secondary to—22 in human meningiomas
-
36 Rey JA, Bello MJ, de Campos JM, Kusak E, Moreno S. Chromosomal involvement secondary to—22 in human meningiomas. Cancer Genet Cytogenet 1988 ; 33: 275–90.
-
(1988)
Cancer Genet Cytogenet
, vol.33
, pp. 275-90
-
-
Rey, JA1
Bello, MJ2
de Campos, JM3
Kusak, E4
Moreno, S.5
-
37
-
-
0026627772
-
Loss of heterozygozity for distal markers on 22q in human gliomas
-
37 Rey JA, Bello MJ, Jimenez‐Lara AM et al. Loss of heterozygozity for distal markers on 22q in human gliomas. Int J Cancer 1992 ; 51: 703–6.
-
(1992)
Int J Cancer
, vol.51
, pp. 703-6
-
-
Rey, JA1
Bello, MJ2
Jimenez‐Lara, AM3
-
38
-
-
0028026793
-
The role of clathrin, adaptors and dynamin in endocytosis
-
38 Robinson MS. The role of clathrin, adaptors and dynamin in endocytosis. Current Opin Cell Biol 1994 ; 6: 538–44.
-
(1994)
Current Opin Cell Biol
, vol.6
, pp. 538-44
-
-
Robinson, MS.1
-
39
-
-
0027245423
-
Alteration of a new gene encoding a putative membrane organizing protein causes neurofibromatosis type 2
-
39 Rouleau GA, Merel P, Lutchman M et al. Alteration of a new gene encoding a putative membrane organizing protein causes neurofibromatosis type 2. Nature 1993 ; 363: 515–21.
-
(1993)
Nature
, vol.363
, pp. 515-21
-
-
Rouleau, GA1
Merel, P2
Lutchman, M3
-
40
-
-
0023204436
-
Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22
-
40 Rouleau GA, Wertelecki W, Haines JL et al. Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22. Nature 1987 ; 329: 246–8.
-
(1987)
Nature
, vol.329
, pp. 246-8
-
-
Rouleau, GA1
Wertelecki, W2
Haines, JL3
-
41
-
-
0003720752
-
Pathology of the Tumours of the Nervous System
-
41 Russell DS, Rubinstein LJ. Pathology of the Tumours of the Nervous System. London: Edward Arnold, 1989.
-
(1989)
-
-
Russell, DS1
Rubinstein, LJ.2
-
42
-
-
0027493815
-
Pre‐symptomatic diagnosis for neurofibromatosis two with chromosome 22 markers
-
42 Ruttledge MH, Narod SA, Dumanski JD et al. Pre‐symptomatic diagnosis for neurofibromatosis two with chromosome 22 markers. Neurology 1993 ; 43: 1753–60.
-
(1993)
Neurology
, vol.43
, pp. 1753-60
-
-
Ruttledge, MH1
Narod, SA2
Dumanski, JD3
-
43
-
-
0028264119
-
Evidence for the complete inactivation of the neurofibromatosis type two gene in the majority of sporadic meningiomas
-
43 Ruttledge MH, Sarrazin J, Rangaratnam S et al. Evidence for the complete inactivation of the neurofibromatosis type two gene in the majority of sporadic meningiomas. Nature Genet 1994 ; 6: 180–4.
-
(1994)
Nature Genet
, vol.6
, pp. 180-4
-
-
Ruttledge, MH1
Sarrazin, J2
Rangaratnam, S3
-
44
-
-
0028276445
-
Deletions on chromosome 22 in sporadic meningioma
-
44 Ruttledge MH, Xie Y‐G, Han F‐Y et al. Deletions on chromosome 22 in sporadic meningioma. Genes Chrom Cancer 1994 ; 10: 122–30.
-
(1994)
Genes Chrom Cancer
, vol.10
, pp. 122-30
-
-
Ruttledge, MH1
Xie, Y‐G2
Han, F‐Y3
-
45
-
-
0028122661
-
Report and abstracts of the Fourth International Workshop on Human Chromosome 22 Mapping 1994
-
45 Scambler PJ. Report and abstracts of the Fourth International Workshop on Human Chromosome 22 Mapping 1994. Cytogenet Cell Genet 1994 ; 67: 277–94.
-
(1994)
Cytogenet Cell Genet
, vol.67
, pp. 277-94
-
-
Scambler, PJ.1
-
46
-
-
0009016044
-
Molecular genetic approach to human meningioma: Loss of genes on chromosome 22
-
46 Seizinger BR de Monte S, Atkins L, Gusella JF, Martuza RL. Molecular genetic approach to human meningioma: Loss of genes on chromosome 22. Proc Natl Acad Sci USA 1987 ; 84: 5419–23.
-
(1987)
Proc Natl Acad Sci USA
, vol.84
, pp. 5419-23
-
-
Seizinger, BR1
de Monte, S2
Atkins, L3
Gusella, JF4
Martuza, RL.5
-
47
-
-
0027236088
-
Germline deletion in a neurofibromatosis type two kindred inactivates the NF2 gene and a candidate meningioma locus
-
47 Sanson M, Marineau C, Desmaze C et al. Germline deletion in a neurofibromatosis type two kindred inactivates the NF2 gene and a candidate meningioma locus. Hum Mol Genet 1993 ; 2: 1215–20.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1215-20
-
-
Sanson, M1
Marineau, C2
Desmaze, C3
-
48
-
-
0028907620
-
Neurofibromatosis type 2 (NF2) gene is somatically mutated in mesothelioma but not in lung cancer
-
48 Sekido Y, Pass HI, Bader S et al. Neurofibromatosis type 2 (NF2) gene is somatically mutated in mesothelioma but not in lung cancer. Cancer Res 1995 ; 55: 1227–31.
-
(1995)
Cancer Res
, vol.55
, pp. 1227-31
-
-
Sekido, Y1
Pass, HI2
Bader, S3
-
49
-
-
85120517809
-
Allelic losses on chromosomes; 14: 10, and 1 in atypical meningiomas: agenetic model of meningioma progression
-
49 Simon M, von Detailing A, Larson JJ et al. Allelic losses on chromosomes; 14: 10, and 1 in atypical meningiomas: agenetic model of meningioma progression. Cancer Res: in press.
-
Cancer Res
-
-
Simon, M1
von Detailing, A2
Larson, JJ3
-
50
-
-
0026677578
-
Loss of heterozygozity on the long arm of chromosome 22 in pheo‐chromocytoma
-
50 Tanaka N, Nishisho I, Yamamoto M et al. Loss of heterozygozity on the long arm of chromosome 22 in pheo‐chromocytoma. Genes Chrom Cancer 1992 ; 5: 399–403.
-
(1992)
Genes Chrom Cancer
, vol.5
, pp. 399-403
-
-
Tanaka, N1
Nishisho, I2
Yamamoto, M3
-
51
-
-
0027405720
-
A novel moesin‐, ezrin‐, radixin‐like gene is a candidate for the neurofibromatosis two tumor supressor
-
51 Trofatter JA, MacCollin MM, Rutter JL et al. A novel moesin‐, ezrin‐, radixin‐like gene is a candidate for the neurofibromatosis two tumor supressor. Cell 1993 ; 72: 791–800.
-
(1993)
Cell
, vol.72
, pp. 791-800
-
-
Trofatter, JA1
MacCollin, MM2
Rutter, JL3
-
52
-
-
0027173060
-
A disease associated germline deletion maps the type two neurofibromatosis (NF2) gene between the Ewing sarcoma region and the leukemia inhibitory factor locus
-
52 Watson CJ, Gaunt L, Evans G, Patel K, Harris R, Strachan T. A disease associated germline deletion maps the type two neurofibromatosis (NF2) gene between the Ewing sarcoma region and the leukemia inhibitory factor locus. Hum Molec Genet 1993 ; 2: 701–4.
-
(1993)
Hum Molec Genet
, vol.2
, pp. 701-4
-
-
Watson, CJ1
Gaunt, L2
Evans, G3
Patel, K4
Harris, R5
Strachan, T.6
-
53
-
-
0027328592
-
Cloning of a novel, anonymous gene from a megabase‐range YAC and cosmid contig in the neurofibromatosis type 2/meningioma region on human chromosome 22q12
-
53 Xie Y‐G, Han F‐Y, Peyrard M et al. Cloning of a novel, anonymous gene from a megabase‐range YAC and cosmid contig in the neurofibromatosis type 2/meningioma region on human chromosome 22q12. Human Molec Genet 1993 ; 2: 1361–8.
-
(1993)
Human Molec Genet
, vol.2
, pp. 1361-8
-
-
Xie, Y‐G1
Han, F‐Y2
Peyrard, M3
-
54
-
-
0028936598
-
Frequent loss of heterozygosity at telomeric loci on 22q in sporadic colorectal cancers
-
54 Yana I, Kurahashi H, Nakamori S et al. Frequent loss of heterozygosity at telomeric loci on 22q in sporadic colorectal cancers. Int J Cancer 1995 ; 60: 174–7.
-
(1995)
Int J Cancer
, vol.60
, pp. 174-7
-
-
Yana, I1
Kurahashi, H2
Nakamori, S3
-
55
-
-
0016774120
-
Cytological and cytogenetical studies on brain tumors VI. No evidence for a translocation in 22‐monosomic meningiomas
-
55 Zankl H, Weiss AF, Zang KD. Cytological and cytogenetical studies on brain tumors VI. No evidence for a translocation in 22‐monosomic meningiomas. Humangenetik 1975 ; 30: 343–8.
-
(1975)
Humangenetik
, vol.30
, pp. 343-8
-
-
Zankl, H1
Weiss, AF2
Zang, KD.3
-
56
-
-
0014991020
-
Cytological and cytogenetical studies on brain tumors. III. Phi‐like chromosomes in human meningiomas
-
56 Zankl H, Zang KD. Cytological and cytogenetical studies on brain tumors. III. Phi‐like chromosomes in human meningiomas. Humangenetik 1971 ; 12: 42–9.
-
(1971)
Humangenetik
, vol.12
, pp. 42-9
-
-
Zankl, H1
Zang, KD.2
-
57
-
-
0019154568
-
Correlations between clinical and cytogenetical data in 180 human meningiomas
-
57 Zankl H, Zang KD. Correlations between clinical and cytogenetical data in 180 human meningiomas. Cancer Genet Cytogenet 1980 ; 1: 351–56.
-
(1980)
Cancer Genet Cytogenet
, vol.1
, pp. 351-56
-
-
Zankl, H1
Zang, KD.2
|