Abnormal X Chromosomes in Man: Origin, Behavior and Effects

Overview

Journal Humangenetik

Specialty Genetics

Date 1974 Jan 1

PMID 4475024

Citations 57

Authors

E THERMAN

K PATAU

Affiliations

Soon will be listed here.

Citing Articles

Heterogeneous gene expression from the inactive X chromosome: an X-linked gene that escapes X inactivation in some human cell lines but is inactivated in others.

Carrel L, Willard H Proc Natl Acad Sci U S A. 1999; 96(13):7364-9.

PMID: 10377420 PMC: 22091. DOI: 10.1073/pnas.96.13.7364.

Duplication of the short arm of the X chromosome in mother and daughter.

Martinez J, Batista D, Kearns W, Wertelecki W Hum Genet. 1993; 91(4):395-400.

PMID: 8500796 DOI: 10.1007/BF00217366.

Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations.

Wolff D, Brown C, Schwartz S, Duncan A, Surti U, Willard H Am J Hum Genet. 1994; 55(1):87-95.

PMID: 8023855 PMC: 1918222.

Primary and secondary nonrandom X chromosome inactivation in early female mouse embryos carrying Searle's translocation T(X; 16)16H.

Takagi N Chromosoma. 1980; 81(3):439-59.

PMID: 7449570 DOI: 10.1007/BF00368155.

Gonadal dysgenesis in a patient with an X;3 translocation: case report and review.

Carpenter N, Say B, Browning D J Med Genet. 1980; 17(3):216-21.

PMID: 7401133 PMC: 1048550. DOI: 10.1136/jmg.17.3.216.

References

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