X-exome sequencing in Finnish families with intellectual disability--four novel mutations and two novel syndromic phenotypes

Added 219 days ago (28.04.2021)
Authors: Anju K Philips; Auli Sirén; Kristiina Avela; Mirja Somer; Maarit Peippo; Minna Ahvenainen; Fatma Doagu; Maria Arvio; Helena Kääriäinen; Hilde Van Esch; Guy Froyen; Stefan A Haas; Hao Hu; Vera M Kalscheuer; Irma Järvelä
Read article