A p.P30L Mutation at the CYP21A2 Gene in Macedonian Patients with Nonclassical Congenital Adrenal Hyperplasia
Anastasovska, V, Kocova, E, Kocova, M
Novel genotype in two siblings with 5-α-reductase 2 deficiency: Different clinical course due to the time of diagnosis
Kocova, M, Plaseska-Karanfilska, D, Noveski, P, Kuzmanovska, M
Organochloride Pesticides in Macedonian Girls With Premature Sexual Development
Krstevska-Konstantinova, M, Kocova, M, Charlier, C, Bourguignon, J
Intron 2 Splice Mutation at CYP21 Gene in Patients with Congenital Adrenal Hyperplasia in the Republic of Macedonia
Anastasovska, V, Kocova, M
Analysis of the SRY Gene in Turner Syndrome Patients from the Republic of Macedonia
Papazovska-Cherepnalkovski, A, Koceva, S, Kocova, M
Clinical variability in two Macedonian families with Arterial tortuosity syndrome
Kocova, M, Kacarska, R, Kuzevska-Maneva, K, Prijic, S, Lazareska, M, Dordoni, C, Ritelli, M, Colombi, M
Molecular Analysis of a Family With Congenital Adrenal Hyperplasia - Genotype/Phenotype Discrepancy
Anastasovska, V, Kocova, M
The Many Faces of Oral-Facial-Digital Syndrome
Sukarova-Angelovska, E, Angelkova, N, Palcevska-Kocevska, S, Kocova, M
Genetic spectrum of neonatal diabetes
Kocova, M