APA

Hrčková G., Jankó V., Kytnarová J., Čižmárová M., Tesařová M., Košťálová Ľ., Virgová D., Dallos T., Hána V., Lebl J., Zeman J. & Kovács L. (20170619). Two novel mutations in seven Czech and Slovak kindreds with familial neurohypophyseal diabetes insipidus-benefit of genetic testing. : European journal of pediatrics.

Chicago

Hrčková Gabriela, Jankó Viktor, Kytnarová Jitka, Čižmárová Michaela, Tesařová Markéta, Košťálová Ľudmila, Virgová Daniela, Dallos Tomáš, Hána Václav, Lebl Jan, Zeman Jiří and Kovács László. 20170619. Two novel mutations in seven Czech and Slovak kindreds with familial neurohypophyseal diabetes insipidus-benefit of genetic testing. : European journal of pediatrics.

Harvard

Hrčková G., Jankó V., Kytnarová J., Čižmárová M., Tesařová M., Košťálová Ľ., Virgová D., Dallos T., Hána V., Lebl J., Zeman J. and Kovács L. (20170619). Two novel mutations in seven Czech and Slovak kindreds with familial neurohypophyseal diabetes insipidus-benefit of genetic testing. : European journal of pediatrics.

MLA

Hrčková Gabriela, Jankó Viktor, Kytnarová Jitka, Čižmárová Michaela, Tesařová Markéta, Košťálová Ľudmila, Virgová Daniela, Dallos Tomáš, Hána Václav, Lebl Jan, Zeman Jiří and Kovács László. Two novel mutations in seven Czech and Slovak kindreds with familial neurohypophyseal diabetes insipidus-benefit of genetic testing. : European journal of pediatrics. 20170619.