Genetic spectrum of neonatal diabetes by Kocova M

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Intron 2 Splice Mutation at CYP21 Gene in Patients with Congenital Adrenal Hyperplasia in the Republic of Macedonia by Anastasovska V, Kocova M

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Molecular Analysis of a Family With Congenital Adrenal Hyperplasia - Genotype/Phenotype Discrepancy by Anastasovska V, Kocova M

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Analysis of the SRY Gene in Turner Syndrome Patients from the Republic of Macedonia by Papazovska-Cherepnalkovski A, Koceva S, Kocova M

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A p.P30L Mutation at the CYP21A2 Gene in Macedonian Patients with Nonclassical Congenital Adrenal Hyperplasia by Anastasovska V, Kocova E, Kocova M

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Organochloride Pesticides in Macedonian Girls With Premature Sexual Development by Krstevska-Konstantinova M, Kocova M, Charlier C, Bourguignon J

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The Many Faces of Oral-Facial-Digital Syndrome by Sukarova-Angelovska E, Angelkova N, Palcevska-Kocevska S, Kocova M

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Novel genotype in two siblings with 5-α-reductase 2 deficiency: Different clinical course due to the time of diagnosis by Kocova M, Plaseska-Karanfilska D, Noveski P, Kuzmanovska M

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Clinical variability in two Macedonian families with Arterial tortuosity syndrome by Kocova M, Kacarska R, Kuzevska-Maneva K, Prijic S, Lazareska M, Dordoni C, Ritelli M, Colombi M

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Disease progression and search for monogenic diabetes among children with new onset type 1 diabetes negative for ICA, GAD- and IA-2 Antibodies by Pörksen, S, Laborie, L, Nielsen, L, Louise Max Andersen, M, Sandal, T, De Wet, H, Schwarcz, E, Aman, J, Swift, P, Kocova, M, Schönle, E, de Beaufort, C, Hougaard, P, Ashcroft, F, Molven, A, Knip, M, Mortensen, H, Hansen, L, Njølstad, P