Utkus A - Search Results

1

SOX9 p.Lys106Glu mutation causes acampomelic campomelic dysplasia: Prenatal and postnatal clinical findings.

Preiksaitiene E, Benušienė E, Matulevičienė A, Grigalionienė K, Utkus A, Kučinskas V. Preiksaitiene E, et al. Among authors: utkus a. Am J Med Genet A. 2016 Mar;170(3):781-4. doi: 10.1002/ajmg.a.37466. Epub 2015 Nov 24. Am J Med Genet A. 2016. PMID: 26602066 No abstract available.

2

Duplication of segment 1p21 following paternal insertional translocation, ins(6;1)(q25;p13.3p22.1).

Utkus A, Sorokina I, Kucinskas V, Röthlisberger B, Balmer D, Brecevic L, Schinzel A. Utkus A, et al. J Med Genet. 1999 Jan;36(1):73-6. J Med Genet. 1999. PMID: 9950373 Free PMC article.

3

Human anotocephaly (aprosopus, acrania-synotia) in the Vilnius anatomical collection.

Utkus A, Kazakevicius R, Ptasekas R, Kucinskas V, Beckwith JB, Opitz JM. Utkus A, et al. Am J Med Genet. 2001 Jun 15;101(2):163-71. doi: 10.1002/ajmg.1320. Am J Med Genet. 2001. PMID: 11391661

4

Few associations of candidate genes with nonsyndromic orofacial clefts in the population of Lithuania.

Morkūniené A, Steponaviciūt D, Utkus A, Kucinskas V. Morkūniené A, et al. Among authors: utkus a. J Appl Genet. 2007;48(1):89-91. doi: 10.1007/BF03194663. J Appl Genet. 2007. PMID: 17272867

5

Recombinant chromosome 14 due to maternal pericentric inversion.

Sliuzas V, Utkus A, Kucinskas V. Sliuzas V, et al. Among authors: utkus a. J Appl Genet. 2008;49(2):205-7. doi: 10.1007/BF03195614. J Appl Genet. 2008. PMID: 18436995

6

Variation in FGF1, FOXE1, and TIMP2 genes is associated with nonsyndromic cleft lip with or without cleft palate.

Nikopensius T, Kempa I, Ambrozaitytė L, Jagomägi T, Saag M, Matulevičienė A, Utkus A, Krjutškov K, Tammekivi V, Piekuse L, Akota I, Barkane B, Krumina A, Klovins J, Lace B, Kučinskas V, Metspalu A. Nikopensius T, et al. Among authors: utkus a. Birth Defects Res A Clin Mol Teratol. 2011 Apr;91(4):218-25. doi: 10.1002/bdra.20791. Epub 2011 Apr 1. Birth Defects Res A Clin Mol Teratol. 2011. PMID: 21462296

7

A novel de novo 1.8 Mb microdeletion of 17q21.33 associated with intellectual disability and dysmorphic features.

Preiksaitiene E, Männik K, Dirse V, Utkus A, Ciuladaite Z, Kasnauskiene J, Kurg A, Kučinskas V. Preiksaitiene E, et al. Among authors: utkus a. Eur J Med Genet. 2012 Nov;55(11):656-9. doi: 10.1016/j.ejmg.2012.07.008. Epub 2012 Jul 27. Eur J Med Genet. 2012. PMID: 22842074

8

Two new de novo interstitial duplications covering 2p14-p22.1: clinical and molecular analysis.

Kasnauskiene J, Cimbalistiene L, Utkus A, Ciuladaite Z, Preiksaitiene E, Pečiulytė A, Kučinskas V. Kasnauskiene J, et al. Among authors: utkus a. Cytogenet Genome Res. 2013;139(1):52-8. doi: 10.1159/000342544. Epub 2012 Oct 2. Cytogenet Genome Res. 2013. PMID: 23036992

9

A new single gene deletion on 2q34: ERBB4 is associated with intellectual disability.

Kasnauskiene J, Ciuladaite Z, Preiksaitiene E, Utkus A, Peciulyte A, Kučinskas V. Kasnauskiene J, et al. Among authors: utkus a. Am J Med Genet A. 2013 Jun;161A(6):1487-90. doi: 10.1002/ajmg.a.35911. Epub 2013 Apr 30. Am J Med Genet A. 2013. PMID: 23633123

10

Heterogeneity of oral clefts in relation to associated congenital anomalies.

Matulevičienė A, Preikšaitienė E, Linkevičienė L, Radavičius M, Molytė A, Utkus A, Kučinskas V. Matulevičienė A, et al. Among authors: utkus a. Medicina (Kaunas). 2013;49(2):61-6. Medicina (Kaunas). 2013. PMID: 23888340 Free article.

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