De La ChapelleA.: XX sex chromosomes in human male: first case. Acta Med. Scand., 175; supl. 412, 25–38 (1964).
2.
BorghiA., FortiG., FusiS., BigozziV., MontaleE., SimoniG., RossellaF.: La sindrome del maschio XX. Recent Progr. Med., 64; 152–201 (1978).
3.
HamertonJ. L., CanningM., RayM., SmithS.: A cytogenetic survey of 14.069 new born infants. Incidence of chromosome abnormalities. Clin. Genet., 8; 223–243 (1975).
4.
PolaniP. E.: Complete sex inversion. Gender difference, p. 18. ed. by OunstedL. and TaylorD. C.Churchill-Livingstone Publ., Edinburgh & London1982.
5.
MidgeleyA. J.: Radioimmunoassay: a method for HCG and human LH. Endrocrinol., 79; 10–15 (1966).
6.
MidgeleyA. J.: Radioimmunoassay: a method for human FSH. J. Clin. Endocrinol. Metab., 27; 295–299 (1967).
OhnoS.: The role of HY antigen in primary sex determination. J.A.M.A., 239; 217–222 (1978)
10.
LindstenJ., BergstrandC. G., TillingerK.G., SchwarzacherH.G., TiepoloL., MuldalS., HökfeltB.: A clinical and cytogenetical study of three patients with male phenotype and apparent XX sex chromosome constitution. Acta Endocrinol., Suppl., 52; 91–112 (1966).
11.
DonaldR. A., EspinerE. A.: The plasma gonadotropin response to gonadotropin-releasing hormone in patients with primary hypogonadism. J. Clin. Endocrinol. Metab., 39; 364–369 (1974).
12.
SilerT. M.YenS. S. C.: Augmented gonadotropin response to synthetic LRF in hypogonadal state. J. Clin. Endocrinol. Metab., 37: 491–494 (1973).
13.
RothJ. C., KelchR. P., KaplanS. L., GrumbachM. M.: FSH and LH response to LH-RF in prepubertal and pubertal children, adult males and patients with hypogonadotropic and hypergonadotropic hypogonadism. J. Clin. Endocrinol. Metab., 35; 926–930 (1972).
