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Page 1
An additional case of 9p syndrome.
Latos-Bielenska A, Krawczynski M, Ignys I, Wolnik-Brzozowska D. Latos-Bielenska A, et al. Among authors: wolnik brzozowska d. Acta Anthropogenet. 1983;7(4):391-5. Acta Anthropogenet. 1983. PMID: 6680318
Frequency of 22q11.2 microdeletion in children with congenital heart defects in western poland.
Wozniak A, Wolnik-Brzozowska D, Wisniewska M, Glazar R, Materna-Kiryluk A, Moszura T, Badura-Stronka M, Skolozdrzy J, Krawczynski MR, Zeyland J, Bobkowski W, Slomski R, Latos-Bielenska A, Siwinska A. Wozniak A, et al. Among authors: wolnik brzozowska d. BMC Pediatr. 2010 Dec 6;10:88. doi: 10.1186/1471-2431-10-88. BMC Pediatr. 2010. PMID: 21134246 Free PMC article.
Differences between predicted and established diagnoses of Smith-Lemli-Opitz syndrome in the Polish population: underdiagnosis or loss of affected fetuses?
Jezela-Stanek A, Ciara E, Małunowicz E, Chrzanowska K, Latos-Bieleńska A, Krajewska-Walasek M; Smith-Lemli-Opitz syndrome Collaborative Group. Jezela-Stanek A, et al. J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S241-8. doi: 10.1007/s10545-010-9132-4. Epub 2010 Jun 16. J Inherit Metab Dis. 2010. PMID: 20556518
[Klippel-Trenaunay disease in a 15-month-old girl].
Krawczyński M, Wolnik-Brzozowska D. Krawczyński M, et al. Among authors: wolnik brzozowska d. Wiad Lek. 1983 Mar 15;36(6):497-500. Wiad Lek. 1983. PMID: 6306932 Polish. No abstract available.