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	1.	Relatives with opposite chromosome constitutions, rec(10)dup(10p)inv(10)(p15.1q26.12) and rec(10)dup(10q)inv(10)(p15.1q26.12), due to a familial pericentric inversion. [electronic resource] by Ciuladaite, Zivile Preiksaitiene, Egle Utkus, Algirdas Kučinskas, Vaidutis Producer: 20150204 In: Cytogenetic and genome research vol. 144 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	None [electronic resource] by Pranckėnienė, Laura Preikšaitienė, Eglė Gueneau, Lucie Reymond, Alexandre Kučinskas, Vaidutis Publication details: Genomics insights 2019 In: Genomics insights vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	16p13.11-p12.3 Microdeletion identified in a patient with sagittal craniosynostosis and developmental delay. [electronic resource] by Maldžienė, Živilė Bulanovaitė, Elena Aleksiūnienė, Beata Utkus, Algirdas Preiksaitiene, Egle Producer: 20200204 In: Clinical dysmorphology vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	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)
	5.	A case report of familial 4q13.3 microdeletion in three individuals with syndromic intellectual disability. [electronic resource] by Maldžienė, Živilė Vaitėnienė, Evelina M Aleksiūnienė, Beata Utkus, Algirdas Preikšaitienė, Eglė Producer: 20210510 In: BMC medical genomics vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Recurrent fetal syndromic spina bifida associated with 3q26.1-qter duplication and 5p13.33-pter deletion due to familial balanced rearrangement. [electronic resource] by Preiksaitiene, Egle Benušienė, Eglė Ciuladaite, Zivile Šliužas, Vytautas Mikštienė, Violeta Kučinskas, Vaidutis Producer: 20170418 In: Taiwanese journal of obstetrics & gynecology vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	A de novo Pericentric Inversion in Chromosome 4 Associated with Disruption of PITX2 and a Microdeletion in 4p15.2 in a Patient with Axenfeld-Rieger Syndrome and Developmental Delay. [electronic resource] by Maldžienė, Živilė Preikšaitienė, Eglė Ignotienė, Salomėja Kapitanova, Natalija Utkus, Algirdas Kučinskas, Vaidutis Producer: 20170925 In: Cytogenetic and genome research vol. 151 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome. [electronic resource] by Pranckėnienė, Laura Bumbulienė, Žana Dasevičius, Darius Utkus, Algirdas Kučinskas, Vaidutis Preikšaitienė, Eglė Producer: 20200309 In: Journal of pediatric and adolescent gynecology vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	SOX9 p.Lys106Glu mutation causes acampomelic campomelic dysplasia: Prenatal and postnatal clinical findings. [electronic resource] by Preiksaitiene, Egle Benušienė, Eglė Matulevičienė, Aušra Grigalionienė, Kristina Utkus, Algirdas Kučinskas, Vaidutis Producer: 20161104 In: American journal of medical genetics. Part A vol. 170 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	A new single gene deletion on 2q34: ERBB4 is associated with intellectual disability. [electronic resource] by Kasnauskiene, Jurate Ciuladaite, Zivile Preiksaitiene, Egle Utkus, Algirdas Peciulyte, Agnė Kučinskas, Vaidutis Producer: 20160415 In: American journal of medical genetics. Part A vol. 161A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	ETV6 and NOTCH1 germline variants in adult acute leukemia. [electronic resource] by Dirse, Vaidas Norvilas, Rimvydas Gineikiene, Egle Matuzevičienė, Rėda Griskevicius, Laimonas Preiksaitiene, Egle Producer: 20190125 In: Leukemia & lymphoma vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Mental retardation and autism associated with recurrent 16p11.2 microdeletion: incomplete penetrance and variable expressivity. [electronic resource] by Ciuladaitė, Zivilė Kasnauskienė, Jūratė Cimbalistienė, Loreta Preikšaitienė, Eglė Patsalis, Philippos C Kučinskas, Vaidutis Producer: 20120208 In: Journal of applied genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Clinical and molecular characterization of a second case of 7p22.1 microduplication. [electronic resource] by Preiksaitiene, Egle Kasnauskiene, Jurate Ciuladaite, Zivile Tumiene, Birute Patsalis, Philippos C Kučinskas, Vaidutis Producer: 20121026 In: American journal of medical genetics. Part A vol. 158A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Heterogeneity of oral clefts in relation to associated congenital anomalies. [electronic resource] by Matulevičienė, Aušra Preikšaitienė, Eglė Linkevičienė, Laura Radavičius, Marijus Molytė, Alma Utkus, Algirdas Kučinskas, Vaidutis Producer: 20140527 In: Medicina (Kaunas, Lithuania) vol. 49 Availability: No items available. Save to lists Add to cart (remove)
	15.	Features of KAT6B-related disorders in a patient with 10q22.1q22.3 deletion. [electronic resource] by Preiksaitiene, Egle Tumienė, Birutė Maldžienė, Živilė Pranckevičienė, Erinija Morkūnienė, Aušra Utkus, Algirdas Kučinskas, Vaidutis Producer: 20171201 In: Ophthalmic genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Considering specific clinical features as evidence of pathogenic copy number variants. [electronic resource] by Preiksaitiene, Egle Molytė, Alma Kasnauskiene, Jurate Ciuladaite, Zivile Utkus, Algirdas Patsalis, Philippos C Kučinskas, Vaidutis Producer: 20150406 In: Journal of applied genetics vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	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)
	18.	R368X mutation in MID1 among recurrent mutations in patients with X-linked Opitz G/BBB syndrome. [electronic resource] by Preiksaitiene, Egle Krasovskaja, Natalija Utkus, Algirdas Kasnauskiene, Jurate Meškienė, Raimonda Paulauskiene, Iveta Valevičienė, Nomeda R Kučinskas, Vaidutis Producer: 20150721 In: Clinical dysmorphology vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Inflammatory myopathy in a patient with Aicardi-Goutières syndrome. [electronic resource] by Tumienė, Birutė Voisin, Norine Preikšaitienė, Eglė Petroška, Donatas Grikinienė, Jurgita Samaitienė, Rūta Utkus, Algirdas Reymond, Alexandre Kučinskas, Vaidutis Producer: 20170217 In: European journal of medical genetics vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	A novel CHD7 variant disrupting acceptor splice site in a patient with mild features of CHARGE syndrome: a case report. [electronic resource] by Siavrienė, Evelina Petraitytė, Gunda Mikštienė, Violeta Rančelis, Tautvydas Maldžienė, Živilė Morkūnienė, Aušra Byčkova, Jekaterina Utkus, Algirdas Kučinskas, Vaidutis Preikšaitienė, Eglė Producer: 20191202 In: BMC medical genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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