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Results of search for 'au:"MIGEON, B R"', page 6 of 7
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Authors
Axelman, J
Beggs, A H
Bias, W B
Childs, B
Corsaro, C M
Do, T T
Driscoll, D J
Gilbert, S F
Haisley-Royster, C
Jacobs, P A
Jani, M
Jeppesen, P
Kaslow, D C
MIGEON, B R
Migeon, B R
Norum, R A
Schmidt, M
Sprenkle, J A
Torchia, B S
Wolf, S F
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Topics
Animals
Cells, Cultured
Clone Cells
Dosage Compensation, Genetic
Female
Fibroblasts
Glucosephosphate Dehydrogenase
Heterozygote
Humans
Hybrid Cells
Karyotyping
Male
Mice
Phenotype
Sex Chromosomes
X Chromosome
cytology
enzymology
genetics
metabolism
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English
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101.
Studies of X inactivation and isodisomy in twins provide further evidence that the X chromosome is not involved in Rett syndrome.
[electronic resource]
by
Migeon, B R
Dunn, M A
Thomas, G
Schmeckpeper, B J
Naidu, S
Producer:
19950413
In:
American journal of human genetics
vol. 56
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102.
Incomplete X chromosome dosage compensation in chorionic villi of human placenta.
[electronic resource]
by
Migeon, B R
Wolf, S F
Axelman, J
Kaslow, D C
Schmidt, M
Producer:
19850625
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 82
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103.
Genetic complementation after fusion of Tay-Sachs and Sandhoff cells.
[electronic resource]
by
Thomas, G H
Taylor, H A
Miller, C S
Axelman, J
Migeon, B R
Producer:
19741009
In:
Nature
vol. 250
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104.
The Barr body is a looped X chromosome formed by telomere association.
[electronic resource]
by
Walker, C L
Cargile, C B
Floy, K M
Delannoy, M
Migeon, B R
Producer:
19910814
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 88
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105.
X-linked Hunter syndrome: the heterozygous phenotype in cell culture.
[electronic resource]
by
Migeon, B R
Sprenkle, J A
Liebaers, I
Scott, J F
Neufeld, E F
Producer:
19771028
In:
American journal of human genetics
vol. 29
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106.
Methylation of the hypoxanthine phosphoribosyltransferase locus on the human X chromosome: implications for X-chromosome inactivation.
[electronic resource]
by
Wolf, S F
Jolly, D J
Lunnen, K D
Friedmann, T
Migeon, B R
Producer:
19840611
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 81
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107.
Molecular characterization of a deleted X chromosome (Xq13.3-Xq21.31) exhibiting random X inactivation.
[electronic resource]
by
Migeon, B R
Stetten, G
Tuck-Muller, C
Axelman, J
Jani, M
Dungy, D
Producer:
19951023
In:
Somatic cell and molecular genetics
vol. 21
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108.
Androgen receptors and metabolism in cultured human fetal fibroblasts.
[electronic resource]
by
Sultan, C
Migeon, B R
Rothwell, S W
Maes, M
Zerhouni, N
Migeon, C J
Producer:
19800514
In:
Pediatric research
vol. 14
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109.
Human thymidine kinase gene locus: assignment to chromosome 17 in a hybrid of man and mouse cells.
[electronic resource]
by
Miller, O J
Allderdice, P W
Miller, D A
Breg, W R
Migeon, B R
Producer:
19710803
In:
Science (New York, N.Y.)
vol. 173
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110.
Localization of loci for hypoxanthine phosphoribosyltransferase and glucose-6-phosphate dehydrogenase and biochemical evidence of nonrandom X chromosome expression from studies of a human X-autosome translocation.
[electronic resource]
by
Pai, G S
Sprenkle, J A
Do, T T
Mareni, C E
Migeon, B R
Producer:
19800926
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 77
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111.
Mechanism of origin of complete hydatidiform moles.
[electronic resource]
by
Jacobs, P A
Wilson, C M
Sprenkle, J A
Rosenshein, N B
Migeon, B R
Producer:
19801124
In:
Nature
vol. 286
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112.
X-linked hypoxanthine-guanine phosphoribosyl transferase deficiency: heterozygote has two clonal populations.
[electronic resource]
by
Migeon, B R
Der Kaloustian, V M
Nyhan, W L
Yough, W J
Childs, B
Producer:
19680523
In:
Science (New York, N.Y.)
vol. 160
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113.
The Hunter syndrome in females: is there an autosomal recessive form of iduronate sulfatase deficiency?
[electronic resource]
by
Neufeld, E F
Liebaers, I
Epstein, C J
Yatziv, S
Milunsky, A
Migeon, B R
Producer:
19771028
In:
American journal of human genetics
vol. 29
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114.
Localization of glucose-6-phosphate dehydrogenase in mouse and man by in situ hybridization: evidence for a single locus and transposition of homologous X-linked genes.
[electronic resource]
by
Martin-DeLeon, P A
Wolf, S F
Persico, G
Toniolo, D
Martini, G
Migeon, B R
Producer:
19850822
In:
Cytogenetics and cell genetics
vol. 39
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115.
Second trimester prenatal diagnosis of epignathus teratoma in ring X chromosome mosaicism with inactive ring X chromosome.
[electronic resource]
by
Witters, I
Moerman, P
Louwagie, D
Van Assche, F A
Migeon, B R
Fryns, J P
Producer:
20020221
In:
Annales de genetique
vol. 44
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116.
Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells.
[electronic resource]
by
Migeon, B R
Moser, H W
Moser, A B
Axelman, J
Sillence, D
Norum, R A
Producer:
19820120
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 78
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117.
Differential expression of steroid sulphatase locus on active and inactive human X chromosome.
[electronic resource]
by
Migeon, B R
Shapiro, L J
Norum, R A
Mohandas, T
Axelman, J
Dabora, R L
Producer:
19821216
In:
Nature
vol. 299
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118.
Selection against lethal alleles in females heterozygous for incontinentia pigmenti.
[electronic resource]
by
Migeon, B R
Axelman, J
Jan de Beur, S
Valle, D
Mitchell, G A
Rosenbaum, K N
Producer:
19890123
In:
American journal of human genetics
vol. 44
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119.
Complete concordance between glucose-6-phosphate dehydrogenase activity and hypomethylation of 3' CpG clusters: implications for X chromosome dosage compensation.
[electronic resource]
by
Wolf, S F
Dintzis, S
Toniolo, D
Persico, G
Lunnen, K D
Axelman, J
Migeon, B R
Producer:
19850221
In:
Nucleic acids research
vol. 12
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120.
Assignment of the haemophilia B (factor IX) locus to the q26-qter region of the X chromosome.
[electronic resource]
by
Boyd, Y
Buckle, V J
Munro, E A
Choo, K H
Migeon, B R
Craig, I W
Producer:
19840813
In:
Annals of human genetics
vol. 48
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