共 43 条
[1]
Mathur A, Stekol L, Schatz D, Et al., The parental origin of the single X chromosome in Turner syndrome: lack of correlation with parental age or clinical phenotype, Am J Hum Genet, 48, (1991)
[2]
Simpson JL, Localizing ovarian determinants through phenotypic-karyotypic deductions, pp. 65-78, (1990)
[3]
Hall JG, Gilchrist DM, Turner syndrome and its variants, Pediatr Clin NA, 37, (1990)
[4]
Fisher EMC, Beer-Romero P, Brown LG, Et al., Homologous ribosomal protein genes on the human Y chromosomes: escape from X inactivation and possible implications for Turner syndrome, Cell, 63, (1990)
[5]
Brown CJ, Ballabio A, Rupert JL, Et al., A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome, Nature, 349, (1991)
[6]
Migeon BR, Jelalian K, Evidence for two active X chromosomes in germ cells of females before meiotic entry, Nature, 269, (1977)
[7]
Hook EB, Warburton D, The distribution of chromosomal genotypes associated with Turner's syndrome: livebirth prevalence rates and evidence for diminished fetal mortality and severity in genotypes associated with structural X abnormalities or mosaicism, Hum Genet, 64, (1983)
[8]
Weiss L, Additional evidence of gradual loss of germ cells in the pathogenesis of streak ovaries in Turner's syndrome, J Med Genet, 8, (1971)
[9]
Lisker R, Jimenez R, Larrea F, Et al., Cytogenetic and endocrine studies in a 45,X female subject with spontaneous sexual development, Am J Obstet Gynecol, 133, (1979)
[10]
Conte FA, Grumbach MM, Kaplan SL, A diphasic pattern of gonadotropin secretion in patients with the syndrome of gonadal dysgenesis, J Clin Endocrinol Metab, 40, (1975)