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J. Mann, A. Valdmanis, S. Capps, R. Puite (1965)
A CASE OF PRIMARY AMENORRHEA WITH A TRANSLOCATION INVOLVING CHROMOSOMES OF GROUPS B AND C.American journal of human genetics, 17
PatriciaA. Jacobs, D. Harnden, W. Brown, J. Goldstein, H. Close, T. Macgregor, N. Maclean, J. Strong (1960)
Abnormalities involving the X chromosome in women.Lancet, 1 7136
A. Morishima, M. Grumbach, J. Taylor (1962)
Asynchronous duplication of human chromosomes and the origin of sex chromatin.Proceedings of the National Academy of Sciences of the United States of America, 48
Ernest Beutlek, Mary Yeh, Virgil Fairbanks (1962)
The normal human female as a mosaic of X-chromosome activity: studies using the gene for C-6-PD-deficiency as a marker.Proceedings of the National Academy of Sciences of the United States of America, 48
G. Stohr (1946)
A case of primary amenorrhea.The Journal of clinical endocrinology and metabolism, 6
S. Ohno, B. Cattanach (1962)
Cytological study of an X-autosome translocation in Mus musculus.Cytogenetics, 1
D. Mukerjee, W. Burdette (1966)
Multiple Congenital Anomalies Associated with a Ring 3 Chromosome and Translocated 3/X ChromosomeNature, 212
J. Salzmann, R. Demars, P. Benke (1968)
Single-allele expression at an X-linked hyperuricemia locus in heterozygous human cells.Proceedings of the National Academy of Sciences of the United States of America, 60 2
(1963)
Presumptive iso - chromosome for the long arm of the X in man . Analysis of five females
Ohno Ohno, Lyon Lyon (1965)
Cytological study of Searle's X ‐autosome translocation in Mus musculusChromosoma (Berl.), 16
M. Lyon (1961)
Gene Action in the X-chromosome of the Mouse (Mus musculus L.)Nature, 190
(1964)
The nature, origin and genetic implications of structural abnormalities in man
R. Davidson, H. Nitowsky, B. Childs (1963)
DEMONSTRATION OF TWO POPULATIONS OF CELLS IN THE HUMAN FEMALE HETEROZYGOUS FOR GLUCOSE-6-PHOSPHATE DEHYDROGENASE VARIANTS.Proceedings of the National Academy of Sciences of the United States of America, 50
L. Russell (1961)
Genetics of Mammalian Sex ChromosomesScience, 133
L. Russell (1963)
Mammalian X-Chromosome Action: Inactivation Limited in Spread and in Region of OriginScience, 140
J. Lindsten, M. Fraccaro, D. Ikkos, K. Kaijser, H. Klinger, R. Luft (1963)
Presumptive isochromosomes for the long arm of X in man. Analysis of five familiesAnnals of Human Genetics, 26
(1968)
Single - allele expression at an X - linked hyperuricemia locus 372 -3 . 861 - 3 . Cytogenetics 1 , 129 - 40
(1963)
Mammalian X-chromosome action: inactivation limited in spread and in region of SALZMANN
(1963)
Presumptive isochromosome for the long arm of the X in man
S. Muldal, C. Gilbert, L. Lajtha, J. Lindsten, J. Rowley, M. Fraccaro (1963)
TRITIATED THYMIDINE INCORPORATION IN AN ISOCHROMOSOME FOR THE LONG ARM OF THE X CHROMOSOME IN MANThe Lancet, 281
Ingemar Gustavsson, M. Fraccaro, L. Tiepolo, J. Lindsten (1968)
Presumptive X-Autosome Translocation in a Cow : Preferential Inactivation of the Normal X ChromosomeNature, 218
F. Giannelli (1963)
The pattern of X-chromosome deoxy-ribonucleic acid synthesis in two women with abnormal sex-chromosome complements.Lancet, 1 7286
B. Danes, A. Bearn (1967)
HURLER'S SYNDROME: A GENETIC STUDY OF CLONES IN CELL CULTURE WITH PARTICULAR REFERENCE TO THE LYON HYPOTHESISThe Journal of Experimental Medicine, 126
E. Beutler, M. Yeh, V. Fairbanks (1962)
THE NORMAL HUMAN FEMALE AS A MOSAIC OF X-CHROMOSOME ACTIVITY: STUDIES USING THE GENE FOR G-6-PD-DEFICIENCY AS A MARKERProceedings of the National Academy of Sciences of the United States of America, 48
Evidence for X / X chromosome translocation in humans BY ANIL K. SINHA AND JAMES J. NORA Departments of Pediatrics, Pathology and Division of Experimental Biology Baylor College of Medicine and Texas Childrenâs Hospital, Houston, Texas, U . S . A . The phenotypic effects of an X/autosome translocation in mice were among the chief sources of evidence that led to the formulation of the single-active-X hypothesis (Lyon, 1961; Russell, 1961; Russell, 1963). Even though cytological examinations of such a stock of mice have shown an X-autosome insertion (Ohno & Cattanach, 1962) rather than a typical translocation, reports are available to suggest the occurrence of X/autosome translocations in humans (Mann, Valdmanis, Capps & Puite, 1965; Mukherjee & Burdette, 1966), as well as in other stocks of mice (Ohno & Lyon, 1965). Recent studies have also shown that, in the cow, the segments of an autosome may be translocated simultaneously to an X-chromosome and an autosomal member of the complement (Gustavsson, Fraccaro, Tupolo & Lindsten, 1968). The individual X-chromosomes of all these X autosome translocation bearing mammals do not suggest a random mode of differentiation in accordance with the single-active-X hypothesis. Whether or not this hypothesis is applicable to
Annals of Human Genetics – Wiley
Published: Oct 1, 1969
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