APA

Obermannova B., Banghova K., Sumník Z., Dvorakova H. M., Betka J., Fencl F., Kolouskova S., Cinek O. & Lebl J. (20090727). Unusually severe phenotype of neonatal primary hyperparathyroidism due to a heterozygous inactivating mutation in the CASR gene. : European journal of pediatrics.

Chicago

Obermannova Barbora, Banghova Karolina, Sumník Zdenek, Dvorakova Hana M, Betka Jan, Fencl Filip, Kolouskova Stanislava, Cinek Ondrej and Lebl Jan. 20090727. Unusually severe phenotype of neonatal primary hyperparathyroidism due to a heterozygous inactivating mutation in the CASR gene. : European journal of pediatrics.

Harvard

Obermannova B., Banghova K., Sumník Z., Dvorakova H. M., Betka J., Fencl F., Kolouskova S., Cinek O. and Lebl J. (20090727). Unusually severe phenotype of neonatal primary hyperparathyroidism due to a heterozygous inactivating mutation in the CASR gene. : European journal of pediatrics.

MLA

Obermannova Barbora, Banghova Karolina, Sumník Zdenek, Dvorakova Hana M, Betka Jan, Fencl Filip, Kolouskova Stanislava, Cinek Ondrej and Lebl Jan. Unusually severe phenotype of neonatal primary hyperparathyroidism due to a heterozygous inactivating mutation in the CASR gene. : European journal of pediatrics. 20090727.