APA

Vuorela P., Ala-Mello S., Saloranta C., Penttinen M., Pöyhönen M., Huoponen K., Borozdin W., Bausch B., Botzenhart E. M., Wilhelm C., Kääriäinen H. & Kohlhase J. (20080116). Molecular analysis of the CHD7 gene in CHARGE syndrome: identification of 22 novel mutations and evidence for a low contribution of large CHD7 deletions. : Genetics in medicine : official journal of the American College of Medical Genetics.

Chicago

Vuorela Pia, Ala-Mello Sirpa, Saloranta Carola, Penttinen Maila, Pöyhönen Minna, Huoponen Kirsi, Borozdin Wiktor, Bausch Birke, Botzenhart Elke M, Wilhelm Christian, Kääriäinen Helena and Kohlhase Jürgen. 20080116. Molecular analysis of the CHD7 gene in CHARGE syndrome: identification of 22 novel mutations and evidence for a low contribution of large CHD7 deletions. : Genetics in medicine : official journal of the American College of Medical Genetics.

Harvard

Vuorela P., Ala-Mello S., Saloranta C., Penttinen M., Pöyhönen M., Huoponen K., Borozdin W., Bausch B., Botzenhart E. M., Wilhelm C., Kääriäinen H. and Kohlhase J. (20080116). Molecular analysis of the CHD7 gene in CHARGE syndrome: identification of 22 novel mutations and evidence for a low contribution of large CHD7 deletions. : Genetics in medicine : official journal of the American College of Medical Genetics.

MLA

Vuorela Pia, Ala-Mello Sirpa, Saloranta Carola, Penttinen Maila, Pöyhönen Minna, Huoponen Kirsi, Borozdin Wiktor, Bausch Birke, Botzenhart Elke M, Wilhelm Christian, Kääriäinen Helena and Kohlhase Jürgen. Molecular analysis of the CHD7 gene in CHARGE syndrome: identification of 22 novel mutations and evidence for a low contribution of large CHD7 deletions. : Genetics in medicine : official journal of the American College of Medical Genetics. 20080116.