References
Bartsch-Sandhoff, M., Terinde, R., Wiegelmann, W., Scholz, W.: Karyotyp-Phenotyp-Korrelation bei einem 46,X,del(X)(p22)-Befund. Hum. Genet. 31, 263–270 (1976)
Fraccaro, M., Maraschio, P., Pasquali, F., Scappaticci, S.: Women heterozygous for deficiency of the (p21→pter) region of the X chromosome are fertile. Hum. Genet. 39, 283–292 (1977)
Giraud, F., Hartung, M., Mattei, J.-F., Bachelet, Y., Mattei, M. G.: Délétion partielle du bras court d'un chromosome X. Arch. Fr. Pediatr. 31, 717–724 (1974)
Hoo, J. J.: Cytogenetic evidence for evolution of X chromosome inactivation. Lancet 1975I, 1299–1300
Hoo, J. J.: Clinical consequence of Xp-. Hum. Genet. 46, 349–351 (1979)
Kaiser, P., Zabel, B., Hansen, S., Daume, E.: Short arm deletion of an X chromosome, 46,XXp-. Hum. Genet. 32, 89–100 (1976)
Pitrinelli, P., Antonelli, A., Gabellini, P., Gigliani, F., Marcucci, L., Nicoletti, B.: Partial deletion of the X chromosome in gonadal dysgenesis 46,X,del(X)(p22) identified by BUdR treatment. Hum. Genet. 45, 351–354 (1978)
Tiepolo, L., Zuffardi, O., Rodewald, A.: Nullisomy for the distal portion of Xp in a male child with X/Y translocation. Hum. Genet. 39, 277–281 (1977)
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Hoo, J.J. A note on the Xp-. Hum Genet 50, 339–340 (1979). https://doi.org/10.1007/BF00399401
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00399401