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Results of search for 'au:"MIGEON, B R"', page 1 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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1.
Short arm deletions in group E and chromosomal "deletion" syndromes.
[electronic resource]
by
Migeon, B R
Producer:
19661017
In:
The Journal of pediatrics
vol. 69
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2.
Stability of X chromosomal inactivation in human somatic cells.
[electronic resource]
by
Migeon, B R
Producer:
19721214
In:
Nature
vol. 239
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3.
Selection and cell communication as determinants of female phenotype.
[electronic resource]
by
Migeon, B R
Producer:
19790816
In:
Basic life sciences
vol. 12
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4.
X-linked hypoxanthine-guanine phosphoribosyl transferase deficiency: detection of heterozygotes by selective medium.
[electronic resource]
by
Migeon, B R
Producer:
19701223
In:
Biochemical genetics
vol. 4
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5.
Hybridization of somatic cells derived from mouse and syrian hamster: evolution of karyotype and enzyme studies.
[electronic resource]
by
Migeon, B R
Producer:
19690515
In:
Biochemical genetics
vol. 1
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6.
X-chromosome inactivation: molecular mechanisms and genetic consequences.
[electronic resource]
by
Migeon, B R
Producer:
19941020
In:
Trends in genetics : TIG
vol. 10
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7.
NICHD conference. Role of DNA methylation in X inactivation and the fragile X syndrome.
[electronic resource]
by
Migeon, B R
Producer:
19930930
In:
American journal of medical genetics
vol. 46
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8.
Insights into X chromosome inactivation from studies of species variation, DNA methylation and replication, and vice versa.
[electronic resource]
by
Migeon, B R
Producer:
19910222
In:
Genetical research
vol. 56
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9.
Studies of skin fibroblasts from 10 families with HGPRT deficiency, with reference in X-chromosomal inactivation.
[electronic resource]
by
Migeon, B R
Producer:
19710823
In:
American journal of human genetics
vol. 23
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10.
Selection of epithelial cells in culture by D-valine medium.
[electronic resource]
by
Migeon, B R
Producer:
19810623
In:
Birth defects original article series
vol. 16
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11.
Non-random X chromosome inactivation in mammalian cells.
[electronic resource]
by
Migeon, B R
Producer:
19980821
In:
Cytogenetics and cell genetics
vol. 80
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12.
Concerning the role of X-inactivation and DNA methylation in fragile X syndrome.
[electronic resource]
by
Migeon, B R
Producer:
19920716
In:
American journal of medical genetics
vol. 43
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13.
Glucose-6-phosphate dehydrogenase as a probe for the study of X-chromosome inactivation in hunan females.
[electronic resource]
by
Migeon, B R
Producer:
19831123
In:
Isozymes
vol. 9
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14.
X chromosome inactivation: theme and variations.
[electronic resource]
by
Migeon, B R
Producer:
20040121
In:
Cytogenetic and genome research
vol. 99
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15.
FAMILIAL VARIANT AUTOSOMES: NEW HUMAN CYTOGENETIC MARKERS.
[electronic resource]
by
MIGEON, B R
Producer:
19961201
In:
Bulletin of the Johns Hopkins Hospital
vol. 116
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16.
Some insights into X chromosome inactivation from studies of human cells.
[electronic resource]
by
Migeon, B R
Producer:
19810513
In:
Annales d'endocrinologie
vol. 41
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17.
Somatic cell hybrids: applications relevant to genetic disease.
[electronic resource]
by
Migeon, B R
Producer:
19720214
In:
The Journal of pediatrics
vol. 79
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18.
The postulated X-inactivation center at Xq27 is most reasonably explained by ascertainment bias: heterozygous expression of recessive mutations is a powerful means of detecting unbalanced X inactivation.
[electronic resource]
by
Migeon, B R
Producer:
19930310
In:
American journal of human genetics
vol. 52
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19.
Stability of X chromosomal inactivation in human somatic cells transformed by SV-40.
[electronic resource]
by
Romeo, G
Migeon, B R
Producer:
19751230
In:
Humangenetik
vol. 29
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20.
Fragile X syndrome: search for phenotypic manifestations at loci for hypoxanthine phosphoribosyltransferase and glucose-6-phosphate dehydrogenase.
[electronic resource]
by
Mareni, C
Migeon, B R
Producer:
19811215
In:
American journal of human genetics
vol. 33
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