APA

Philips A. K., Sirén A., Avela K., Somer M., Peippo M., Ahvenainen M., Doagu F., Arvio M., Kääriäinen H., Van Esch H., Froyen G., Haas S. A., Hu H., Kalscheuer V. M. & Järvelä I. (20140926). X-exome sequencing in Finnish families with intellectual disability--four novel mutations and two novel syndromic phenotypes. : Orphanet journal of rare diseases.

Chicago

Philips Anju K, Sirén Auli, Avela Kristiina, Somer Mirja, Peippo Maarit, Ahvenainen Minna, Doagu Fatma, Arvio Maria, Kääriäinen Helena, Van Esch Hilde, Froyen Guy, Haas Stefan A, Hu Hao, Kalscheuer Vera M and Järvelä Irma. 20140926. X-exome sequencing in Finnish families with intellectual disability--four novel mutations and two novel syndromic phenotypes. : Orphanet journal of rare diseases.

Harvard

Philips A. K., Sirén A., Avela K., Somer M., Peippo M., Ahvenainen M., Doagu F., Arvio M., Kääriäinen H., Van Esch H., Froyen G., Haas S. A., Hu H., Kalscheuer V. M. and Järvelä I. (20140926). X-exome sequencing in Finnish families with intellectual disability--four novel mutations and two novel syndromic phenotypes. : Orphanet journal of rare diseases.

MLA

Philips Anju K, Sirén Auli, Avela Kristiina, Somer Mirja, Peippo Maarit, Ahvenainen Minna, Doagu Fatma, Arvio Maria, Kääriäinen Helena, Van Esch Hilde, Froyen Guy, Haas Stefan A, Hu Hao, Kalscheuer Vera M and Järvelä Irma. X-exome sequencing in Finnish families with intellectual disability--four novel mutations and two novel syndromic phenotypes. : Orphanet journal of rare diseases. 20140926.