De novo KMT2D heterozygous frameshift deletion in a newborn with a congenital heart anomaly
Stangler Herodež, Š, Marčun Varda, N, N, Kokalj Vokač, Krgović, D
MTHFR C677T and A1298C Genotypes and Haplotypes in Slovenian Couples with Unexplained Infertility Problems and in Embryonic Tissues from Spontaneous Abortions
Stangler Herodež, Š, Zagradišnik, B, Erjavec Škerget, A, Zagorac, A, Takač, I, Vlaisavljević, V, Lokar, L, Kokalj Vokač, N
Detection of mutations in the CYP21A2 gene: genotype-phenotype correlation in Slovenian couples with conceiving problems
Stangler Herodež, Š, Fijavž, L, Zagradišnik, B, Kokalj Vokač, N