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The Hillside Journal of Clinical Psychiatry|January 1, 1984
Therapeutic milieu and clinical improvementM Dumic, T E GiftArchives of Disease in Childhood|March 1, 1982
Premature thelarche: a possible adrenal disorderM Dumic, M Tajic, D Mardesic, et al.American Journal of Medical Genetics|July 15, 1992
Sparse hair and multiple endocrine disorders in two women heterozygous for adrenoleukodystrophyM Dumic, N Gubarev, N Sikic, et al.Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|August 6, 2015
Low bone mineral density for age/osteoporosis in triple A syndrome-an overlooked symptom of unexplained etiologyM Dumic, N R Putarek, V Kusec, et al.Metabolism: Clinical and Experimental|October 1, 1980
A liver urocanase deficiencyZ Kalafatic, K Lipovac, Z Jezerinac, et al.Molecular Endocrinology (Baltimore, Md.)|May 1, 1991
A mutation (Pro-30 to Leu) in CYP21 represents a potential nonclassic steroid 21-hydroxylase deficiency alleleM T Tusie-Luna, P W Speiser, M Dumic, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|July 16, 1993
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 mellitusA Stavljenic-Rukavina, J Sertic, B Salzer, et al.Hormone Research|December 12, 2001
Extraovarian steroid cell tumor 'not otherwise specified' as a rare cause of virilization in twelve-year-old girlM Dumic, V Simunic, J Ilic-Forko, et al.Archives of Oral Biology|November 28, 2009
Characteristics of the craniofacial complex in Turner syndromeJ Dumancic, Z Kaic, M Lapter Varga, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|November 11, 2005
Pregnancy outcomes in women with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiencyM Dumic, N Janjanin, J Ille, et al.Pageof 2