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	1.	A de novo 1q22q23.1 Interstitial Microdeletion in a Girl with Intellectual Disability and Multiple Congenital Anomalies Including Congenital Heart Defect. [electronic resource] by Aleksiūnienė, Beata Preiksaitiene, Egle Morkūnienė, Aušra Ambrozaitytė, Laima Utkus, Algirdas Producer: 20180419 In: Cytogenetic and genome research vol. 154 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	X-linked juvenile retinoschisis: phenotypic and genetic characterization. [electronic resource] by Strupaitė, Rasa Ambrozaitytė, Laima Cimbalistienė, Loreta Ašoklis, Rimvydas Utkus, Algirdas Publication details: International journal of ophthalmology 2018 In: International journal of ophthalmology vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Insights Into [electronic resource] by Pranckėnienė, Laura Jakaitienė, Audronė Ambrozaitytė, Laima Kavaliauskienė, Ingrida Kučinskas, Vaidutis Publication details: Frontiers in genetics 2018 In: Frontiers in genetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Novel mutation in a patient with late onset GLUT1 deficiency syndrome. [electronic resource] by Juozapaite, Sandra Praninskiene, Ruta Burnyte, Birute Ambrozaityte, Laima Skerliene, Birute Producer: 20170330 In: Brain & development vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Novel human genome variants associated with alcohol use disorders identified in a Lithuanian cohort. [electronic resource] by Baronas, Karolis Rančelis, Tautvydas Pranculis, Aidas Domarkienė, Ingrida Ambrozaitytė, Laima Kučinskas, Vaidutis Publication details: Acta medica Lituanica 2018 In: Acta medica Lituanica vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Identification of genetic causes of congenital neurodevelopmental disorders using genome wide molecular technologies. [electronic resource] by Preikšaitienė, Eglė Ambrozaitytė, Laima Maldžienė, Živilė Morkūnienė, Aušra Cimbalistienė, Loreta Rančelis, Tautvydas Utkus, Algirdas Kučinskas, Vaidutis Publication details: Acta medica Lituanica 2016 In: Acta medica Lituanica vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Analysis of Lithuanian CYP2D6 polymorphism and its relevance to psychiatric care of the local population. [electronic resource] by Dlugauskas, Edgaras Strumila, Robertas Lengvenyte, Aiste Ambrozaityte, Laima Dagyte, Evelina Molyte, Alma Navickas, Alvydas Utkus, Algirdas Producer: 20190513 In: Nordic journal of psychiatry vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Examinations of maternal uniparental disomy and epimutations for chromosomes 6, 14, 16 and 20 in Silver-Russell syndrome-like phenotypes. [electronic resource] by Sachwitz, Jana Strobl-Wildemann, Getrud Fekete, György Ambrozaitytė, Laima Kučinskas, Vaidutis Soellner, Lukas Begemann, Matthias Eggermann, Thomas Producer: 20160511 In: BMC medical genetics vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Analysis of pathogenic variants from the ClinVar database in healthy people using next-generation sequencing. [electronic resource] by Rančelis, Tautvydas Arasimavičius, Justas Ambrozaitytė, Laima Kavaliauskienė, Ingrida Domarkienė, Ingrida Karčiauskaitė, Dovilė Kučinskienė, Zita Aušrelė Kučinskas, Vaidutis Producer: 20171214 In: Genetics research vol. 99 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Frame shift mutations of the ZMPSTE24 gene in two siblings with restrictive dermopathy. [electronic resource] by Matulevičienė, Aušra Meškienė, Raimonda Morkūnienė, Aušra Ambrozaitytė, Laima Meškauskas, Raimundas Garunkštienė, Rasa Drazdienė, Nijolė Utkus, Algirdas Kučinskas, Vaidutis Producer: 20160928 In: Clinical dysmorphology vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	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. [electronic resource] by Aleksiūnienė, Beata Matulevičiūtė, Rugilė Matulevičienė, Aušra Burnytė, Birutė Krasovskaja, Natalija Ambrozaitytė, Laima Mikštienė, Violeta Dirsė, Vaidas Utkus, Algirdas Kučinskas, Vaidutis Producer: 20170501 In: Medicine vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Association of BMP4 polymorphisms with non-syndromic cleft lip with or without cleft palate and isolated cleft palate in Latvian and Lithuanian populations. [electronic resource] by Kempa, Inga Ambrozaitytė, Laima Stavusis, Janis Akota, Ilze Barkane, Biruta Krumina, Astrida Matulevičienė, Aušra Utkus, Algirdas Kučinskas, Vaidutis Lace, Baiba Producer: 20160329 In: Stomatologija vol. 16 Availability: No items available. Save to lists Add to cart (remove)
	13.	Classical rather than genetic risk factors account for high cardiovascular disease prevalence in Lithuania: A cross-sectional population study. [electronic resource] by Burokienė, Neringa Domarkienė, Ingrida Ambrozaitytė, Laima Uktverytė, Ingrida Meškienė, Raimonda Karčiauskaitė, Dovilė Kasiulevičius, Vytautas Šapoka, Virginijus Kučinskas, Vaidutis Kučinskienė, Zita Aušrelė Producer: 20180223 In: Advances in medical sciences vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Pathogenic homozygous variant in POMK gene is the cause of prenatally detected severe ventriculomegaly in two Lithuanian families. [electronic resource] by Preiksaitiene, Egle Voisin, Norine Gueneau, Lucie Benušienė, Eglė Krasovskaja, Natalija Blažytė, Evelina Marija Ambrozaitytė, Laima Rančelis, Tautvydas Reymond, Alexandre Kučinskas, Vaidutis Producer: 20210104 In: American journal of medical genetics. Part A vol. 182 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Replication of novel susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 in Estonian and Lithuanian patients. [electronic resource] by Nikopensius, Tiit Ambrozaityte, Laima Ludwig, Kerstin U Birnbaum, Stefanie Jagomägi, Triin Saag, Mare Matuleviciene, Ausra Linkeviciene, Laura Herms, Stefan Knapp, Michael Hoffmann, Per Nöthen, Markus M Kucinskas, Vaidutis Metspalu, Andres Mangold, Elisabeth Producer: 20100106 In: American journal of medical genetics. Part A vol. 149A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	The high frequency of GJB2 gene mutation c.313_326del14 suggests its possible origin in ancestors of Lithuanian population. [electronic resource] by Mikstiene, Violeta Jakaitiene, Audrone Byckova, Jekaterina Gradauskiene, Egle Preiksaitiene, Egle Burnyte, Birute Tumiene, Birute Matuleviciene, Ausra Ambrozaityte, Laima Uktveryte, Ingrida Domarkiene, Ingrida Rancelis, Tautvydas Cimbalistiene, Loreta Lesinskas, Eugenijus Kucinskas, Vaidutis Utkus, Algirdas Producer: 20161019 In: BMC genetics vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Genetic variants in COL2A1, COL11A2, and IRF6 contribute risk to nonsyndromic cleft palate. [electronic resource] by Nikopensius, Tiit Jagomägi, Triin Krjutskov, Kaarel Tammekivi, Veronika Saag, Mare Prane, Inga Piekuse, Linda Akota, Ilze Barkane, Biruta Krumina, Astrida Ambrozaityte, Laima Matuleviciene, Ausra Kucinskiene, Zita Ausrele Lace, Baiba Kucinskas, Vaidutis Metspalu, Andres Producer: 20110104 In: Birth defects research. Part A, Clinical and molecular teratology vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Variation in FGF1, FOXE1, and TIMP2 genes is associated with nonsyndromic cleft lip with or without cleft palate. [electronic resource] by Nikopensius, Tiit Kempa, Inga Ambrozaitytė, Laima Jagomägi, Triin Saag, Mare Matulevičienė, Aušra Utkus, Algirdas Krjutškov, Kaarel Tammekivi, Veronika Piekuse, Linda Akota, Ilze Barkane, Biruta Krumina, Astrida Klovins, Janis Lace, Baiba Kučinskas, Vaidutis Metspalu, Andres Producer: 20110815 In: Birth defects research. Part A, Clinical and molecular teratology vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	KIAA1109 Variants Are Associated with a Severe Disorder of Brain Development and Arthrogryposis. [electronic resource] by Gueneau, Lucie Fish, Richard J Shamseldin, Hanan E Voisin, Norine Tran Mau-Them, Frédéric Preiksaitiene, Egle Monroe, Glen R Lai, Angeline Putoux, Audrey Allias, Fabienne Ambusaidi, Qamariya Ambrozaityte, Laima Cimbalistienė, Loreta Delafontaine, Julien Guex, Nicolas Hashem, Mais Kurdi, Wesam Jamuar, Saumya Shekhar Ying, Lim J Bonnard, Carine Pippucci, Tommaso Pradervand, Sylvain Roechert, Bernd van Hasselt, Peter M Wiederkehr, Michaël Wright, Caroline F Xenarios, Ioannis van Haaften, Gijs Shaw-Smith, Charles Schindewolf, Erica M Neerman-Arbez, Marguerite Sanlaville, Damien Lesca, Gaëtan Guibaud, Laurent Reversade, Bruno Chelly, Jamel Kučinskas, Vaidutis Alkuraya, Fowzan S Reymond, Alexandre Producer: 20181211 In: American journal of human genetics vol. 102 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)