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Identification of eight novel NSD1 mutations in Sotos syndrome.
Kamimura J, Endo Y, Kurotaki N, Kinoshita A, Miyake N, Shimokawa O, Harada N, Visser R, Ohashi H, Miyakawa K, Gerritsen J, Innes AM, Lagace L, Frydman M, Okamoto N, Puttinger R, Raskin S, Resic B, Culic V, Yoshiura K, Ohta T, Kishino T, Ishikawa M, Niikawa N, Matsumoto N. Kamimura J, et al. Among authors: resic b. J Med Genet. 2003 Nov;40(11):e126. doi: 10.1136/jmg.40.11.e126. J Med Genet. 2003. PMID: 14627693 Free PMC article. No abstract available.
A Croatian case of the Schinzel-Giedion syndrome.
Culić V, Resic B, Oorthuys JW, Overweg-Plandsoen WC, Hennekam RC. Culić V, et al. Among authors: resic b. Genet Couns. 1996;7(1):21-5. Genet Couns. 1996. PMID: 8652084
Association of NOS3 tag polymorphisms with hypoxic-ischemic encephalopathy.
Kuzmanić Samija R, Primorac D, Resić B, Lozić B, Krzelj V, Tomasović M, Stoini E, Samanović L, Benzon B, Pehlić M, Boraska V, Zemunik T. Kuzmanić Samija R, et al. Among authors: resic b. Croat Med J. 2011 Jun;52(3):396-402. doi: 10.3325/cmj.2011.52.396. Croat Med J. 2011. PMID: 21674837 Free PMC article.
16 results