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Acute Pre-B Lymphoblastic Leukemia and Congenital Anomalies in a Child with a de Novo 22q11.1q11.22 Duplication.
Balkan J Med Genet. 2018 Oct 29;21(1):87-91. doi: 10.2478/bjmg-2018-0002. eCollection 2018 Jun.
Balkan J Med Genet. 2018.
PMID: 30425917
Free PMC article.
Opposite chromosome constitutions due to a familial translocation t(1;21)(q43;q22) in 2 cousins with development delay and congenital anomalies: A case report.
Aleksiūnienė B, Matulevičiūtė R, Matulevičienė A, Burnytė B, Krasovskaja N, Ambrozaitytė L, Mikštienė V, Dirsė V, Utkus A, Kučinskas V.
Aleksiūnienė B, et al.
Medicine (Baltimore). 2017 Apr;96(16):e6521. doi: 10.1097/MD.0000000000006521.
Medicine (Baltimore). 2017.
PMID: 28422838
Free PMC article.
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A de novo 1q22q23.1 Interstitial Microdeletion in a Girl with Intellectual Disability and Multiple Congenital Anomalies Including Congenital Heart Defect.
Aleksiūnienė B, Preiksaitiene E, Morkūnienė A, Ambrozaitytė L, Utkus A.
Aleksiūnienė B, et al.
Cytogenet Genome Res. 2018;154(1):6-11. doi: 10.1159/000486947. Epub 2018 Feb 9.
Cytogenet Genome Res. 2018.
PMID: 29421787
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A case report of familial 4q13.3 microdeletion in three individuals with syndromic intellectual disability.
Maldžienė Ž, Vaitėnienė EM, Aleksiūnienė B, Utkus A, Preikšaitienė E.
Maldžienė Ž, et al. Among authors: aleksiuniene b.
BMC Med Genomics. 2020 Apr 16;13(1):63. doi: 10.1186/s12920-020-0711-4.
BMC Med Genomics. 2020.
PMID: 32299451
Free PMC article.
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16p13.11-p12.3 Microdeletion identified in a patient with sagittal craniosynostosis and developmental delay.
Maldžienė Ž, Bulanovaitė E, Aleksiūnienė B, Utkus A, Preiksaitiene E.
Maldžienė Ž, et al. Among authors: aleksiuniene b.
Clin Dysmorphol. 2019 Oct;28(4):195-197. doi: 10.1097/MCD.0000000000000285.
Clin Dysmorphol. 2019.
PMID: 31205052
No abstract available.
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