1. Boczkowski, K., Mikkelsen, M.: Fluorescence and autoradiographic studies in patients with Turner's syndrome and 46,XXp- and 46,XXq- karyotypes. J. med. Genet. 10, 350?355 (1973)
2. Davis, J. R., Heine, M. W., Lightner, E. S., Giles, H. R., Graap, R. F.: X-Short arm deletion gonadal dysgenesis in two siblings due to unique translocation (Xp-;16p+). Clin. Genet. 10, 202?207 (1976)
3. Feingold, M., Bossert, W. H.: Normal values for selected physical parameters: an aid to syndrome delineation. Birth Defects X, 1?15 (1974)
4. Goodman, R. M., Gorlin, R. J.: The face in genetic disorders, p. 168. Saint Louis: Mosby 1970
5. Gorlin, R. J., Pindborg, J. J., Cohen, M. M., Jr.: Syndromes of the head and neck, p. 101. New York: McGraw-Hill 1976