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Algirdas Utkus

Showing results (41-50 of 102) with videos related to

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Pediatric Rheumatology Online Journal|March 26, 2016
Perinatal manifestation of mevalonate kinase deficiency and efficacy of anakinraSkaiste Peciuliene, Birute Burnyte, Rymanta Gudaitiene, et al.
Medicina (Kaunas, Lithuania)|July 27, 2013
Heterogeneity of oral clefts in relation to associated congenital anomaliesAušra Matulevičienė, Eglė Preikšaitienė, Laura Linkevičienė, et al.
Medicina (Kaunas, Lithuania)|June 28, 2023
A De Novo 8q22.2q22.3 Interstitial Microdeletion in a Girl with Developmental Delay and Congenital DefectsRuta Kalinauskiene, Deimante Brazdziunaite, Neringa Burokiene, et al.
Children (Basel, Switzerland)|January 26, 2024
Fetal Alcohol Spectrum Disorders and Inadequacy of Care: Importance of Raising Awareness in Clinical PracticeSigita Lesinskienė, Emilijus Žilinskas, Algirdas Utkus, et al.
Cell Biology International|January 13, 2019
Epigenetic alterations in amniotic fluid mesenchymal stem cells derived from normal and fetus-affected gestations: A focus on myogenic and neural differentiationsMonika Gasiūnienė, Aistė Zentelytė, Gražina Treigytė, et al.
Ophthalmic Genetics|November 24, 2016
Features of KAT6B-related disorders in a patient with 10q22.1q22.3 deletionEgle Preiksaitiene, Birutė Tumienė, Živilė Maldžienė, et al.
Genes|October 26, 2024
Utilization of Microfluidic Droplet-Based Methods in Diagnosis and Treatment Methods of Hepatocellular Carcinoma: A ReviewAkvilė Zajanckauskaite, Miah Lingelbach, Dovilė Juozapaitė, et al.
Journal of Applied Genetics|February 19, 2014
Considering specific clinical features as evidence of pathogenic copy number variantsEgle Preiksaitiene, Alma Molytė, Jurate Kasnauskiene, et al.
Biomedicines|February 25, 2022
Perspectives in Sports GenomicsValentina Ginevičienė, Algirdas Utkus, Erinija Pranckevičienė, et al.
American Journal of Medical Genetics. Part A|February 24, 2015
Thiamine responsive megaloblastic anemia syndrome: a novel homozygous SLC19A2 gene mutation identifiedVioleta Mikstiene, Jurgita Songailiene, Jekaterina Byckova, et al.
Pageof 11

Showing results (41-50 of 102) with videos related to

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Pageof 11
Pediatric Rheumatology Online Journal|March 26, 2016
Perinatal manifestation of mevalonate kinase deficiency and efficacy of anakinraSkaiste Peciuliene, Birute Burnyte, Rymanta Gudaitiene, et al.
Medicina (Kaunas, Lithuania)|July 27, 2013
Heterogeneity of oral clefts in relation to associated congenital anomaliesAušra Matulevičienė, Eglė Preikšaitienė, Laura Linkevičienė, et al.
Medicina (Kaunas, Lithuania)|June 28, 2023
A De Novo 8q22.2q22.3 Interstitial Microdeletion in a Girl with Developmental Delay and Congenital DefectsRuta Kalinauskiene, Deimante Brazdziunaite, Neringa Burokiene, et al.
Children (Basel, Switzerland)|January 26, 2024
Fetal Alcohol Spectrum Disorders and Inadequacy of Care: Importance of Raising Awareness in Clinical PracticeSigita Lesinskienė, Emilijus Žilinskas, Algirdas Utkus, et al.
Cell Biology International|January 13, 2019
Epigenetic alterations in amniotic fluid mesenchymal stem cells derived from normal and fetus-affected gestations: A focus on myogenic and neural differentiationsMonika Gasiūnienė, Aistė Zentelytė, Gražina Treigytė, et al.
Ophthalmic Genetics|November 24, 2016
Features of KAT6B-related disorders in a patient with 10q22.1q22.3 deletionEgle Preiksaitiene, Birutė Tumienė, Živilė Maldžienė, et al.
Genes|October 26, 2024
Utilization of Microfluidic Droplet-Based Methods in Diagnosis and Treatment Methods of Hepatocellular Carcinoma: A ReviewAkvilė Zajanckauskaite, Miah Lingelbach, Dovilė Juozapaitė, et al.
Journal of Applied Genetics|February 19, 2014
Considering specific clinical features as evidence of pathogenic copy number variantsEgle Preiksaitiene, Alma Molytė, Jurate Kasnauskiene, et al.
Biomedicines|February 25, 2022
Perspectives in Sports GenomicsValentina Ginevičienė, Algirdas Utkus, Erinija Pranckevičienė, et al.
American Journal of Medical Genetics. Part A|February 24, 2015
Thiamine responsive megaloblastic anemia syndrome: a novel homozygous SLC19A2 gene mutation identifiedVioleta Mikstiene, Jurgita Songailiene, Jekaterina Byckova, et al.
Pageof 11