Ravnik-Glavac M.,2000
Ravnik-Glavac M., Dean M., Glavac D. Two novel missense mutations (R766M and R792G) in exon 13 of the CFTR gene in a patient with congenital bilateral absense of the vas deferens. - Hum.Hered., 2000, v. 50, p. 318-319
Ravnik-Glavac M., Dean M., Glavac D. Two novel missense mutations (R766M and R792G) in exon 13 of the CFTR gene in a patient with congenital bilateral absense of the vas deferens. - Hum.Hered., 2000, v. 50, p. 318-319
