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Two siblings with immunodeficiency, facial abnormalities and chromosomal instability without mutation in DNMT3B gene but liability towards malignancy; a new chromatin disorder delineation?
Polityko A, Khurs O, Rumyantseva N, Naumchik I, Kosyakova N, Tönnies H, Sperling K, Neitzel H, Weise A, Liehr T. Polityko A, et al. Among authors: kosyakova n. Mol Cytogenet. 2010 Mar 8;3:5. doi: 10.1186/1755-8166-3-5. Mol Cytogenet. 2010. PMID: 20211012 Free PMC article.
Heteromorphic variants of chromosome 9.
Kosyakova N, Grigorian A, Liehr T, Manvelyan M, Simonyan I, Mkrtchyan H, Aroutiounian R, Polityko AD, Kulpanovich AI, Egorova T, Jaroshevich E, Frolova A, Shorokh N, Naumchik IV, Volleth M, Schreyer I, Nelle H, Stumm M, Wegner RD, Reising-Ackermann G, Merkas M, Brecevic L, Martin T, Rodríguez L, Bhatt S, Ziegler M, Kreskowski K, Weise A, Sazci A, Vorsanova S, Cioffi Mde B, Ergul E. Kosyakova N, et al. Mol Cytogenet. 2013 Apr 1;6(1):14. doi: 10.1186/1755-8166-6-14. Mol Cytogenet. 2013. PMID: 23547710 Free PMC article.
Complex chromosome rearrangement in a child with microcephaly, dysmorphic facial features and mosaicism for a terminal deletion del(18)(q21.32-qter) investigated by FISH and array-CGH: Case report.
Manolakos E, Kosyakova N, Thomaidis L, Neroutsou R, Weise A, Mihalatos M, Orru S, Kokotas H, Kitsos G, Liehr T, Petersen MB. Manolakos E, et al. Among authors: kosyakova n. Mol Cytogenet. 2008 Nov 11;1:24. doi: 10.1186/1755-8166-1-24. Mol Cytogenet. 2008. PMID: 19014423 Free PMC article.
125 results