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. DOI:10.1159/000133420. PMID1486803.
Christensen JH, Siggaard C, Corydon TJ, et al (January 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. DOI:10.1038/sj.ejhg.5201086. PMID14673472.
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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. DOI:10.1159/000133420. PMID1486803.
Christensen JH, Siggaard C, Corydon TJ, et al (January 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. DOI:10.1038/sj.ejhg.5201086. PMID14673472.
