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References
Chapelle, A., Hortling, H., Niemi, M., and Wennstrom, J. (1964). XX sex chromosomes in a human male. First case.Acta Med. Scand. Suppl., pp. 412–425.
de Grouchy, J., Canivet, J., Canlorbe, P., and Mantel, O. (1967). Deux observations d'homme 46/XX.Ann. Genet. 10 193.
Ferguson-Smith, M. (1966). X-Y chromosomal interchange in the aetiology of true hermaphroditism and of XX Klinefelter's syndrome.Lancet 2 475.
Romberg, M., Clayton, G., and Hsu, T. (1963). Familial true hermaphrodism.J. Clin. Endocrinol. Metab. 33 203.
Sturdevant, A. (1945). A gene inDrosophila melanogaster that transforms females into males.Genetics 30 297.
Therkelsen, A. (1964). Sterile male with the chromosome constitution 46/XX.Cytogenetics 3 207.
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Translated and condensed from “Etude clinique et biologique d'un suject de phenotype male et de formule chromosomique 46,XX.”Ann. Endocrinol. 29: 351–361 (1968).
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Canivet, J., de Grouchy, J. & Mantel, O. A clinical and biological study of a patient of male phenotype and chromosome formula 46XX. Arch Sex Behav 2, 173–176 (1972). https://doi.org/10.1007/BF01541866
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DOI: https://doi.org/10.1007/BF01541866