-
1
-
-
0026523228
-
Telomere shortening associated with chromosome instability is arrested in immortal cells which express telomerase activity
-
Counter, C.M., Avilion, A.A., Le Feuvre, C.E., Stewart, N.G., Greider, C.W., Harley, C.B. and Bacchetti, S. (1992). Telomere shortening associated with chromosome instability is arrested in immortal cells which express telomerase activity. EMBO J. 11: 1921-1929.
-
(1992)
EMBO J.
, vol.11
, pp. 1921-1929
-
-
Counter, C.M.1
Avilion, A.A.2
Le Feuvre, C.E.3
Stewart, N.G.4
Greider, C.W.5
Harley, C.B.6
Bacchetti, S.7
-
2
-
-
0016739638
-
Deletion mapping of the human X chromosome
-
de la Chapelle, A., Schroder, J., Haahtela, T. and Aro, P. (1975). Deletion mapping of the human X chromosome. Hereditas 80: 113-120.
-
(1975)
Hereditas
, vol.80
, pp. 113-120
-
-
De La Chapelle, A.1
Schroder, J.2
Haahtela, T.3
Aro, P.4
-
3
-
-
0023188432
-
Chromosomally abnormal clones and non-random telomeric translocations in cardiac myxomas
-
Dewald, G.W., Dahl, R.J., Spurbeck, J.L., Carney, J.A. and Gordon, H. (1987). Chromosomally abnormal clones and non-random telomeric translocations in cardiac myxomas. Mayo Clin. Proc. 62: 558-567.
-
(1987)
Mayo Clin. Proc.
, vol.62
, pp. 558-567
-
-
Dewald, G.W.1
Dahl, R.J.2
Spurbeck, J.L.3
Carney, J.A.4
Gordon, H.5
-
4
-
-
0028631196
-
High frequency of telomeric association in a family with multiple congenital neoplasia
-
Dhaliwal, M.K., Satya-Prakash, K.L., Davis, P.C. and Pathak, S. (1994). High frequency of telomeric association in a family with multiple congenital neoplasia. In Vivo 8: 1023-1026.
-
(1994)
In Vivo
, vol.8
, pp. 1023-1026
-
-
Dhaliwal, M.K.1
Satya-Prakash, K.L.2
Davis, P.C.3
Pathak, S.4
-
5
-
-
76549210828
-
Karyotype-phenotype correlations in gonadal dysgenesis and their bearing on the pathogenesis of malformations
-
Ferguson-Smith, M.A. (1965). Karyotype-phenotype correlations in gonadal dysgenesis and their bearing on the pathogenesis of malformations. J. Med. Genet. 2: 142-145.
-
(1965)
J. Med. Genet.
, vol.2
, pp. 142-145
-
-
Ferguson-Smith, M.A.1
-
6
-
-
0020030761
-
Premature menopause due to a small deletion in the long arm of the X chromosome: A report of three cases and a review
-
Fitch, N., Victor, J., Richer, C., Pinsky, L. and Sitahal, S. (1982). Premature menopause due to a small deletion in the long arm of the X chromosome: A report of three cases and a review. Am. J. Obstet. Gynecol. 142: 968-972.
-
(1982)
Am. J. Obstet. Gynecol.
, vol.142
, pp. 968-972
-
-
Fitch, N.1
Victor, J.2
Richer, C.3
Pinsky, L.4
Sitahal, S.5
-
7
-
-
0021206827
-
Telomeric association in B-cell lymphoid leukemia
-
Fitzgerald, P.H. and Morris, C.M. (1984). Telomeric association in B-cell lymphoid leukemia. Hum. Genet. 67: 385-390.
-
(1984)
Hum. Genet.
, vol.67
, pp. 385-390
-
-
Fitzgerald, P.H.1
Morris, C.M.2
-
8
-
-
0016161764
-
X-long arm deletion with features of Turner's syndrome
-
Forabosco, A. and Dallapiccola, B. (1974). X-long arm deletion with features of Turner's syndrome (letter). Lancet 2: 403-404.
-
(1974)
Lancet
, vol.2
, pp. 403-404
-
-
Forabosco, A.1
Dallapiccola, B.2
-
9
-
-
0020059758
-
Clinical and cytogenetic aspects of X-chromosome deletions
-
Goldman, B., Polani, P.E., Daker, M.G. and Angell, R.R. (1982). Clinical and cytogenetic aspects of X-chromosome deletions. Clin. Genet. 21: 36-52.
-
(1982)
Clin. Genet.
, vol.21
, pp. 36-52
-
-
Goldman, B.1
Polani, P.E.2
Daker, M.G.3
Angell, R.R.4
-
10
-
-
0025787643
-
Telomere loss: Mitotic clock or genetic time bomb?
-
Harley, C.B. (1991). Telomere loss: Mitotic clock or genetic time bomb? Mutat. Res. 256: 271-282.
-
(1991)
Mutat. Res.
, vol.256
, pp. 271-282
-
-
Harley, C.B.1
-
11
-
-
0027153972
-
Telomeric associations in a patient with B-cell prolymphocytic leukemia
-
Howell, R.T., Kitchen, C. and Standen, G.R. (1993). Telomeric associations in a patient with B-cell prolymphocytic leukemia. Genes Chromosom. Cancer 7: 116-118.
-
(1993)
Genes Chromosom. Cancer
, vol.7
, pp. 116-118
-
-
Howell, R.T.1
Kitchen, C.2
Standen, G.R.3
-
12
-
-
0008668114
-
Cytogenetic studies in primary amenorrhoea
-
Jacobs, P.A., Harnden, D.G., Buckton, K.E., Brown, W.M., King, M.J., McBride, J.A., MacGregor, T.N. and MacLean, N. (1961). Cytogenetic studies in primary amenorrhoea. Lancet 1: 1183-1189.
-
(1961)
Lancet
, vol.1
, pp. 1183-1189
-
-
Jacobs, P.A.1
Harnden, D.G.2
Buckton, K.E.3
Brown, W.M.4
King, M.J.5
McBride, J.A.6
MacGregor, T.N.7
MacLean, N.8
-
13
-
-
33749694690
-
The role of fetal hormones in prenatal development
-
Academic Press, New York
-
Jost, A. (1959-1960). The role of fetal hormones in prenatal development. In: "Harvey Lectures, Series 55". Academic Press, New York pp. 201-225.
-
(1959)
Harvey Lectures, Series 55
, pp. 201-225
-
-
Jost, A.1
-
14
-
-
0015487612
-
A new look at the mechanisms controlling sex differentiation in mammals
-
Jost, A. (1972). A new look at the mechanisms controlling sex differentiation in mammals. John Hopkins Med. J. 130: 38.
-
(1972)
John Hopkins Med. J.
, vol.130
, pp. 38
-
-
Jost, A.1
-
16
-
-
7144223296
-
Gene action in the X-chromosome of the mouse (Mus musculus I.)
-
Lyon, M.F. (1961). Gene action in the X-chromosome of the mouse (Mus musculus I.) Nature 190: 372.
-
(1961)
Nature
, vol.190
, pp. 372
-
-
Lyon, M.F.1
-
17
-
-
0019496026
-
Structural anomalies of the X-chromosome and inactivation center
-
Mattei, M.G., Mattei, J.F., Vidal, J. and Giraud, F. (1981). Structural anomalies of the X-chromosome and inactivation center. Hum. Genet. 56: 401-408.
-
(1981)
Hum. Genet.
, vol.56
, pp. 401-408
-
-
Mattei, M.G.1
Mattei, J.F.2
Vidal, J.3
Giraud, F.4
-
18
-
-
0019992723
-
X long arm deletion with oligomenorrhea
-
Mijin, K., Stolevic, E., Adzic, S., Laca, Z. and Markovic S. (1982). X long arm deletion with oligomenorrhea. J. Med. Genet. 19: 305-306.
-
(1982)
J. Med. Genet.
, vol.19
, pp. 305-306
-
-
Mijin, K.1
Stolevic, E.2
Adzic, S.3
Laca, Z.4
Markovic, S.5
-
19
-
-
0022469505
-
Telomeric fusion in pre T-cell acute lymphoblastic leukemia
-
Morgan, R., Jarzabek, V., Jaffe, J.P., Hecht, B.K., Hecht, F. and Sandberg, A.A. (1986). Telomeric fusion in pre T-cell acute lymphoblastic leukemia. Hum. Genet. 73: 260-262.
-
(1986)
Hum. Genet.
, vol.73
, pp. 260-262
-
-
Morgan, R.1
Jarzabek, V.2
Jaffe, J.P.3
Hecht, B.K.4
Hecht, F.5
Sandberg, A.A.6
-
20
-
-
0017161113
-
Chromosome banding techniques
-
Pathak S. (1976). Chromosome banding techniques. J. Reprod. Med. 17: 25-28.
-
(1976)
J. Reprod. Med.
, vol.17
, pp. 25-28
-
-
Pathak, S.1
-
21
-
-
0023807489
-
Telomeric association: Another characteristic of cancer chromosomes?
-
Pathak, S., Wang, Z., Dhaliwal, M.K. and Sacks, P.C. (1988). Telomeric association: Another characteristic of cancer chromosomes? Cytogenet. Cell. Genet. 47: 227-229.
-
(1988)
Cytogenet. Cell. Genet.
, vol.47
, pp. 227-229
-
-
Pathak, S.1
Wang, Z.2
Dhaliwal, M.K.3
Sacks, P.C.4
-
22
-
-
0028596902
-
Chromosome alterations in cancer development and apoptosis
-
Pathak, S., Dave, B.J. and Gagos, S.H. (1994a). Chromosome alterations in cancer development and apoptosis. In Vivo 8: 843-850.
-
(1994)
In Vivo
, vol.8
, pp. 843-850
-
-
Pathak, S.1
Dave, B.J.2
Gagos, S.H.3
-
23
-
-
0028069227
-
Telomeric association of chromosomes is an early manifestation of programmed cell death
-
Pathak, S., Risin, S., Brown, N.M. and Berry, K. (1994b). Telomeric association of chromosomes is an early manifestation of programmed cell death. Int. J. Oncol. 4: 323-328.
-
(1994)
Int. J. Oncol.
, vol.4
, pp. 323-328
-
-
Pathak, S.1
Risin, S.2
Brown, N.M.3
Berry, K.4
-
24
-
-
84915863322
-
Chromosome phenotypes - Sex chromosomes
-
The Hague, Netherlands, 7-13 September (Clarke Fraser, F. and McKusick, V.A., eds.). Excerpta Medica, Amsterdam and New York
-
Polani, P.E. (1969). Chromosome phenotypes - sex chromosomes. In: "Proceedings of the III International Conference on Congenital Malformations." The Hague, Netherlands, 7-13 September (Clarke Fraser, F. and McKusick, V.A., eds.). Excerpta Medica, Amsterdam and New York, pp. 233-250.
-
(1969)
Proceedings of the III International Conference on Congenital Malformations
, pp. 233-250
-
-
Polani, P.E.1
-
25
-
-
0018407178
-
Partial long arm deletion of one X chromosome in a patient with secondary amenorrhea
-
Ruthner, U., Maschik, S., Friedrich, F. and Breitenecker, G. (1979). Partial long arm deletion of one X chromosome in a patient with secondary amenorrhea. Hum. Genet. 48: 135-137.
-
(1979)
Hum. Genet.
, vol.48
, pp. 135-137
-
-
Ruthner, U.1
Maschik, S.2
Friedrich, F.3
Breitenecker, G.4
-
26
-
-
0019833947
-
Long arm deletion of the X chromosome, 46,X,del(X)(q21), associated with gonadoblastoma
-
Seki, T., Fujimoto, S., Abe, S., Sasaki, M., Kawaguchi, I., Kikukawa, H., Kikuchi, Y. and Ichinoe, K. (1981). Long arm deletion of the X chromosome, 46,X,del(X)(q21), associated with gonadoblastoma. Jpn. J. Hum. Genet. 26: 307-312.
-
(1981)
Jpn. J. Hum. Genet.
, vol.26
, pp. 307-312
-
-
Seki, T.1
Fujimoto, S.2
Abe, S.3
Sasaki, M.4
Kawaguchi, I.5
Kikukawa, H.6
Kikuchi, Y.7
Ichinoe, K.8
-
27
-
-
0018196567
-
X-autosome translocations: A review
-
Summit, R.L., Tipton, R.E., Wilroy Jr., R.S., Martens, P.R. and Phelman, J.P. (1978). X-autosome translocations: A review: Birth Defects 14: 219-247.
-
(1978)
Birth Defects
, vol.14
, pp. 219-247
-
-
Summit, R.L.1
Tipton, R.E.2
Wilroy Jr., R.S.3
Martens, P.R.4
Phelman, J.P.5
-
29
-
-
0016176571
-
Abnormal X chromosome in man: Origin, behavior and effects
-
Therman, E. and Patau, K. (1974). Abnormal X chromosome in man: Origin, behavior and effects. Hum. Genet. 25: 1-16.
-
(1974)
Hum. Genet.
, vol.25
, pp. 1-16
-
-
Therman, E.1
Patau, K.2
-
30
-
-
0015949158
-
Center for Barr body condensation on the proximal part of human Xq: A hypothesis
-
Therman, E., Sarto, G.E. and Patau, K. (1974). Center for Barr body condensation on the proximal part of human Xq: A hypothesis. Chromosoma 44: 361-366.
-
(1974)
Chromosoma
, vol.44
, pp. 361-366
-
-
Therman, E.1
Sarto, G.E.2
Patau, K.3
-
31
-
-
0018318613
-
Position of a human X inactivation center on Xq
-
Therman, E., Sarto, G.E., Palmer, C.G., Kallio, H. and Denniston, C. (1979). Position of a human X inactivation center on Xq. Hum. Genet. 50: 59-64.
-
(1979)
Hum. Genet.
, vol.50
, pp. 59-64
-
-
Therman, E.1
Sarto, G.E.2
Palmer, C.G.3
Kallio, H.4
Denniston, C.5
-
32
-
-
0020039712
-
Structural anomalies of the X chromosome: Personal observations and review of non-mosaic cases
-
Wyss, D., Delozier, C.D., Daniell, J. and Engel, E. (1982). Structural anomalies of the X chromosome: Personal observations and review of non-mosaic cases. Clin. Genet. 21: 145-159.
-
(1982)
Clin. Genet.
, vol.21
, pp. 145-159
-
-
Wyss, D.1
Delozier, C.D.2
Daniell, J.3
Engel, E.4
|