M Dumić

A Mutation (Pro-30 to Leu) in<i>CYP</i>21 Represents a Potential Nonclassic Steroid 21-Hydroxylase Deficiency Allele

Maria-Teresa Tusie-Luna, Phyllis Speiser, M Dumić et al. · Molecular Endocrinology · 1991 · 183 citations · Full text

Ethnic-specific distribution of mutations in 716 patients with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency

Robert C. Wilson, Saroj Nimkarn, M Dumić et al. · Molecular Genetics and Metabolism · 2007 · 135 citations · Full text

Ethnic-specific Distribution, Urology, Adrenal Gland +10

An update on the frequency of nonclassic deficiency of adrenal 21-hydroxylase in the Yugoslav population

M Dumić, L Brkljacić, Phyllis Speiser et al. · European Journal of Endocrinology · 1990 · 33 citations

Adrenal Gland, Mendelian Disorder, Genetic Disorder +15

Polymorphism of apolipoprotein E, lipoprotein(a), and other lipoproteins in children with type I diabetes.

Branka Salzer, A Stavljenić, Günther Jürgens et al. · PubMed · 1993 · 19 citations

Genetic Epidemiology, Hyperlipidemia, Apo E 3/2 +17

Apolipoprotein E phenotypes and genotypes as determined by polymerase chain reaction using allele-specific oligonucleotide probes and the amplification refractory mutation system in children with insulin-dependent diabetes mellitus

Ana Stavljenić-Rukavina, Jadranka Sertić, Branka Salzer et al. · Clinica Chimica Acta · 1993 · 19 citations

Metabolic Syndrome, Allelic Variant, Allele-specific Oligonucleotide Probes +11