-
1
-
-
2742580231
-
Monozygotic twins discordant for Duchenne muscular dystrophy. Evidence for mirror X-chromosome inactivation
-
Tokyo, Japan
-
Abaddi N, Phillipe C, Cherry M, Gilgenkrantz S, Tome F, Kaplan JC, Fardeau M (1992): Monozygotic twins discordant for Duchenne muscular dystrophy. Evidence for mirror X-chromosome inactivation. Proceedings of the 7th International Congress on Twin Studies, Tokyo, Japan.
-
(1992)
Proceedings of the 7th International Congress on Twin Studies
-
-
Abaddi, N.1
Phillipe, C.2
Cherry, M.3
Gilgenkrantz, S.4
Tome, F.5
Kaplan, J.C.6
Fardeau, M.7
-
2
-
-
0025233690
-
A highly informative X-chromosome probe, M27β, can be used for the determination of tumour clonality
-
Abrahamson G, Fraser N, Boyd Y, Craig I, Wainscoat J (1990): A highly informative X-chromosome probe, M27β, can be used for the determination of tumour clonality. Br J Haematol 74:371-372.
-
(1990)
Br J Haematol
, vol.74
, pp. 371-372
-
-
Abrahamson, G.1
Fraser, N.2
Boyd, Y.3
Craig, I.4
Wainscoat, J.5
-
3
-
-
0345128844
-
Polymorphic DNA region adjacent to the 5' end of the human insulin gene
-
Bell G, Karam J, Rutter W (1981): Polymorphic DNA region adjacent to the 5' end of the human insulin gene. Proc Natl Acad Sci USA 78:5759-5763.
-
(1981)
Proc Natl Acad Sci USA
, vol.78
, pp. 5759-5763
-
-
Bell, G.1
Karam, J.2
Rutter, W.3
-
4
-
-
0027410902
-
X chromosome inactivation and the diagnosis of X linked disease in females
-
Brown R, Brown G (1993): X chromosome inactivation and the diagnosis of X linked disease in females. J Med Genet 30:177-184.
-
(1993)
J Med Genet
, vol.30
, pp. 177-184
-
-
Brown, R.1
Brown, G.2
-
5
-
-
0023024584
-
Duchenne muscular dystrophy in one of monozygotic twin girls
-
Burn J, Povey S, Boyd Y, Munro E, West L, Harper K, Thomas D (1986): Duchenne muscular dystrophy in one of monozygotic twin girls. J Med Genet 23:494-500.
-
(1986)
J Med Genet
, vol.23
, pp. 494-500
-
-
Burn, J.1
Povey, S.2
Boyd, Y.3
Munro, E.4
West, L.5
Harper, K.6
Thomas, D.7
-
6
-
-
0024691032
-
Isolation and characterisation of a human variable copy number tandem repeat as Xcen-p11.22
-
Fraser N, Boyd Y, Craig I (1989): Isolation and characterisation of a human variable copy number tandem repeat as Xcen-p11.22. Genomics 5:144-148.
-
(1989)
Genomics
, vol.5
, pp. 144-148
-
-
Fraser, N.1
Boyd, Y.2
Craig, I.3
-
7
-
-
26144480008
-
Skewed and non-random X-inactivation are more common in MZ twin females
-
Goodship JA, Burn J, Speer A (1992): Skewed and non-random X-inactivation are more common in MZ twin females. Am J Hum Genet 51[Suppl A]:467.
-
(1992)
Am J Hum Genet
, vol.51
, Issue.SUPPL. A
, pp. 467
-
-
Goodship, J.A.1
Burn, J.2
Speer, A.3
-
8
-
-
0030042952
-
X-inactivation patterns in monozygotic and Dizygotic Female Twins
-
Goodship J, Carter J, Burn J (1996): X-inactivation patterns in monozygotic and Dizygotic Female Twins. Am J Med Genet 61: 205-208.
-
(1996)
Am J Med Genet
, vol.61
, pp. 205-208
-
-
Goodship, J.1
Carter, J.2
Burn, J.3
-
9
-
-
0024849533
-
X-chromosome inactivation in the human cytotrophoblast
-
Harrison KB (1989): X-chromosome inactivation in the human cytotrophoblast. Cytogenet Cell Genet 52:37-41.
-
(1989)
Cytogenet Cell Genet
, vol.52
, pp. 37-41
-
-
Harrison, K.B.1
-
10
-
-
0022442180
-
Analysis of the human α-globin gene cluster reveals a highly informative genetic locus
-
Higgs D, Wainscoat J, Flint J, Hill A, Thein S, Nicholls R, Teal H, Ayyub H, Peto T, Falusi A, Jarman A, Clegg J, Weatherall D (1986): Analysis of the human α-globin gene cluster reveals a highly informative genetic locus. Proc Natl Acad Sci USA 83: 5165-5169.
-
(1986)
Proc Natl Acad Sci USA
, vol.83
, pp. 5165-5169
-
-
Higgs, D.1
Wainscoat, J.2
Flint, J.3
Hill, A.4
Thein, S.5
Nicholls, R.6
Teal, H.7
Ayyub, H.8
Peto, T.9
Falusi, A.10
Jarman, A.11
Clegg, J.12
Weatherall, D.13
-
11
-
-
0024312392
-
Dystrophin analysis in clonal myoblasts derived from a Duchenne muscular dystrophy carrier
-
Hurko O, Hoffman E, McKee L, Johns D, Kunkel L (1989): Dystrophin analysis in clonal myoblasts derived from a Duchenne muscular dystrophy carrier. Am J Hum Genet 44:820-826.
-
(1989)
Am J Hum Genet
, vol.44
, pp. 820-826
-
-
Hurko, O.1
Hoffman, E.2
McKee, L.3
Johns, D.4
Kunkel, L.5
-
12
-
-
0026645782
-
Opposite patterns of X inactivation in MZ twins discordant for red-green color deficiency
-
Jorgensen A, Philip J, Christensen B, Raskind W, Matsushita M, Motulsky A (1992): Opposite patterns of X inactivation in MZ twins discordant for red-green color deficiency. Am J Hum Genet 51:291-298.
-
(1992)
Am J Hum Genet
, vol.51
, pp. 291-298
-
-
Jorgensen, A.1
Philip, J.2
Christensen, B.3
Raskind, W.4
Matsushita, M.5
Motulsky, A.6
-
13
-
-
2742513208
-
Monozygotic twins discordant for the fragile X syndrome (FXS)
-
Kruyer H, Mila M, Glover G, Castellani-Bel S, Carbonelli P (1993): Monozygotic twins discordant for the fragile X syndrome (FXS). Am J Hum Genet 53[Suppl 3]:A465.
-
(1993)
Am J Hum Genet
, vol.53
, Issue.3 SUPPL.
-
-
Kruyer, H.1
Mila, M.2
Glover, G.3
Castellani-Bel, S.4
Carbonelli, P.5
-
14
-
-
0026023199
-
Different phenotypic expression of Fabry disease in female monozygotic twins
-
Levada T, Giordano F, Maret F, Marguery MC, Bazex J, Salvayre R (1991): Different phenotypic expression of Fabry disease in female monozygotic twins. J Inher Metab Dis 14:105-106.
-
(1991)
J Inher Metab Dis
, vol.14
, pp. 105-106
-
-
Levada, T.1
Giordano, F.2
Maret, F.3
Marguery, M.C.4
Bazex, J.5
Salvayre, R.6
-
15
-
-
0025733349
-
Discordance of muscular dystrophy in monozygotic female twins
-
Lupski J, Garcia C, Zoghbi H, Hoffman E, Fenwick R (1991): Discordance of muscular dystrophy in monozygotic female twins. Am J Med Genet 40:354-364.
-
(1991)
Am J Med Genet
, vol.40
, pp. 354-364
-
-
Lupski, J.1
Garcia, C.2
Zoghbi, H.3
Hoffman, E.4
Fenwick, R.5
-
16
-
-
0343558600
-
Adrenoleucodystrophy: Evidence for X-linkage, inactivation and selection favoring the mutant allele in heterozygous cells
-
Migeon B, Moser H, Moser A, Axelman J, Sillence D, Norum R (1981): Adrenoleucodystrophy: Evidence for X-linkage, inactivation and selection favoring the mutant allele in heterozygous cells. Proc Natl Acad Sci U S A 78:5066-5070.
-
(1981)
Proc Natl Acad Sci U S A
, vol.78
, pp. 5066-5070
-
-
Migeon, B.1
Moser, H.2
Moser, A.3
Axelman, J.4
Sillence, D.5
Norum, R.6
-
17
-
-
0021811416
-
Incomplete X chromosome dosage compensation in chorionic villi of human placenta
-
Migeon BR, Wolf SF, Axelman J, Kaslow DC, Schmidt M (1985): Incomplete X chromosome dosage compensation in chorionic villi of human placenta. Proc Natl Acad Sci U S A 82:3390-3394.
-
(1985)
Proc Natl Acad Sci U S A
, vol.82
, pp. 3390-3394
-
-
Migeon, B.R.1
Wolf, S.F.2
Axelman, J.3
Kaslow, D.C.4
Schmidt, M.5
-
18
-
-
0023104845
-
Variable number tandem repeat (VNTR) markers for human gene mapping
-
Nakamura Y, Leppert M, O'Connell P, Wolfe R, Holm T, Culver M, Martin C, Fujimoto E, Hoff M, Kumlin E, White R (1987): Variable number tandem repeat (VNTR) markers for human gene mapping. Science 235:1616-1622.
-
(1987)
Science
, vol.235
, pp. 1616-1622
-
-
Nakamura, Y.1
Leppert, M.2
O'Connell, P.3
Wolfe, R.4
Holm, T.5
Culver, M.6
Martin, C.7
Fujimoto, E.8
Hoff, M.9
Kumlin, E.10
White, R.11
-
19
-
-
0025407462
-
Invited editorial: Do twin Lyons have larger spots?
-
Nance W (1990): Invited editorial: Do twin Lyons have larger spots? Am J Hum Genet 46:646-348.
-
(1990)
Am J Hum Genet
, vol.46
, pp. 646-1348
-
-
Nance, W.1
-
21
-
-
0025253465
-
Prenatal test for X-linked severe combined immunodeficiency by analysis of maternal X-chromosome inactivation and linkage analysis
-
Puck J, Krause C, Pucj S, Buckley R, Conley M (1990): Prenatal test for X-linked severe combined immunodeficiency by analysis of maternal X-chromosome inactivation and linkage analysis. N Engl J Med 322:1063-1066.
-
(1990)
N Engl J Med
, vol.322
, pp. 1063-1066
-
-
Puck, J.1
Krause, C.2
Pucj, S.3
Buckley, R.4
Conley, M.5
-
22
-
-
0025329757
-
Skewed X inactivation in a female MZ twin results in Duchenne muscular dystrophy
-
Richards CS, Watkins SC, Hoffman EP, Schneider NR, Milsark IW, Katz KS, Cook JD, Kunkel LM, Cortada JM (1990a): Skewed X inactivation in a female MZ twin results in Duchenne muscular dystrophy. Am J Hum Genet 46:672-681.
-
(1990)
Am J Hum Genet
, vol.46
, pp. 672-681
-
-
Richards, C.S.1
Watkins, S.C.2
Hoffman, E.P.3
Schneider, N.R.4
Milsark, I.W.5
Katz, K.S.6
Cook, J.D.7
Kunkel, L.M.8
Cortada, J.M.9
-
23
-
-
1842343958
-
Skewed X-inactivation in normal monozygotic twin pairs
-
Richards CS, Hall JG, Falterman ML, Nance WE (1990b): Skewed X-inactivation in normal monozygotic twin pairs. Am J Hum Genet 47[Suppl A]:105.
-
(1990)
Am J Hum Genet
, vol.47
, Issue.SUPPL. A
, pp. 105
-
-
Richards, C.S.1
Hall, J.G.2
Falterman, M.L.3
Nance, W.E.4
-
24
-
-
0027405405
-
X-chromosome inactivation occurs at different times in different tissues of the post-implantation mouse embryo
-
Tan SS, Williams EA, Tam PPL (1993): X-chromosome inactivation occurs at different times in different tissues of the post-implantation mouse embryo. Nature Genet 3:170-174.
-
(1993)
Nature Genet
, vol.3
, pp. 170-174
-
-
Tan, S.S.1
Williams, E.A.2
Tam, P.P.L.3
-
25
-
-
0021964205
-
Frequency and replication status of the fragile X, fra(X)(q27-28), in a pair of monozygotic twins of markedly differing intelligence
-
Tuckerman E, Webb T, Bunday SE (1985): Frequency and replication status of the fragile X, fra(X)(q27-28), in a pair of monozygotic twins of markedly differing intelligence. J Med Genet 22: 85-91.
-
(1985)
J Med Genet
, vol.22
, pp. 85-91
-
-
Tuckerman, E.1
Webb, T.2
Bunday, S.E.3
-
26
-
-
0027051409
-
Female twin with Hunter disease due to nonrandom inactivation of the X-chromosome
-
Winchester B, Young E, Geddes S, Genet S, Hurst J, Middleton-Price H, Williams N, Webb M, Habel A, Malcolm S (1992): Female twin with Hunter disease due to nonrandom inactivation of the X-chromosome. Am J Med Genet 44:834-838.
-
(1992)
Am J Med Genet
, vol.44
, pp. 834-838
-
-
Winchester, B.1
Young, E.2
Geddes, S.3
Genet, S.4
Hurst, J.5
Middleton-Price, H.6
Williams, N.7
Webb, M.8
Habel, A.9
Malcolm, S.10
-
27
-
-
0027410123
-
In situ hybridization shows direct evidence of skewed X inactivation in one of monozygotic twin females manifesting Duchenne muscular dystrophy
-
Zneimer S, Schneider N, Richards C (1993): In situ hybridization shows direct evidence of skewed X inactivation in one of monozygotic twin females manifesting Duchenne muscular dystrophy. Am J Med Genet 45:601-605.
-
(1993)
Am J Med Genet
, vol.45
, pp. 601-605
-
-
Zneimer, S.1
Schneider, N.2
Richards, C.3
|