Rao VV, Löffler C, Battey J, Hansmann I (1992). „The human gene for oxytocin-neurophysin I (OXT) is physically mapped to chromosome 20p13 by in situ hybridization”. Cytogenet. Cell Genet. 61 (4): 271—3. PMID1486803. doi:10.1159/000133420.
Christensen JH; Siggaard C; Corydon TJ; et al. (2004). „Six novel mutations in the arginine vasopressin gene in 15 kindreds with autosomal dominant familial neurohypophyseal diabetes insipidus give further insight into the pathogenesis”. Eur. J. Hum. Genet. 12 (1): 44—51. PMID14673472. doi:10.1038/sj.ejhg.5201086.CS1 одржавање: Експлицитна употреба et al. (веза)
nih.gov
ncbi.nlm.nih.gov
Rao VV, Löffler C, Battey J, Hansmann I (1992). „The human gene for oxytocin-neurophysin I (OXT) is physically mapped to chromosome 20p13 by in situ hybridization”. Cytogenet. Cell Genet. 61 (4): 271—3. PMID1486803. doi:10.1159/000133420.
Christensen JH; Siggaard C; Corydon TJ; et al. (2004). „Six novel mutations in the arginine vasopressin gene in 15 kindreds with autosomal dominant familial neurohypophyseal diabetes insipidus give further insight into the pathogenesis”. Eur. J. Hum. Genet. 12 (1): 44—51. PMID14673472. doi:10.1038/sj.ejhg.5201086.CS1 одржавање: Експлицитна употреба et al. (веза)
