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"Boris Peterlin"
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Otopalatodigital Syndrome Type I: Novel Characteristics and Prenatal Manifestations in two Siblings (2019-12)
I. Joksic, G. Cuturilo, A. Jurisic, S. Đuričić, B. Peterlin, M. Mijovic, N. Orlic Karadzov, A. Egic, Z. Milovanovic, Otopalatodigital Syndrome Type I: Novel Characteristics and Prenatal Manifestations in two Siblings, BALKAN JOURNAL OF MEDICAL GENETICS, Vol. 22, No. 2, pp. 83 - 88, Dec, 2019 -
A novel variant in the LIPA gene associated with distinct phenotype. (2022)
A. Sarajlija, L. Armengol, A. Maver, I. Kitić, D. Prokić, M. Ćehić, S. Đuričić, B. Peterlin, A novel variant in the LIPA gene associated with distinct phenotype., BALKAN JOURNAL OF MEDICAL GENETICS, Vol. 25, No. 1, pp. 93 - 100, 2022